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dbVar

Database of genomic structural variation

nsv5543526

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:36

Publication(s):Byrska-Bishop et al. 2022

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view

Submitted genomic99,934,255-99,934,290

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5543526	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	99,934,255	99,934,290
nsv5543526	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	102,696,537	102,696,572

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17025536	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17025536	Submitted genomic		NC_000009.12:g.999 34255_99934290ins3 15	GRCh38 (hg38)		NC_000009.12	Chr9	99,934,255	99,934,290
nssv17025536	Remapped	Perfect	NC_000009.11:g.102 696537_102696572in s315	GRCh37.p13	First Pass	NC_000009.11	Chr9	102,696,537	102,696,572

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17025536	<0.001	1	6404

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