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dbVar

Database of genomic structural variation

nsv5622358

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 95 SVs from 25 studies. See in: genome view

Submitted genomic13,331,032-13,331,032

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5622358	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	13,331,032	13,331,032
nsv5622358	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	13,372,532	13,372,532

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17120225	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17120225	Submitted genomic		NC_000003.12:g.133 31032_13331033ins2 54	GRCh38 (hg38)		NC_000003.12	Chr3	13,331,032	13,331,032
nssv17120225	Remapped	Perfect	NC_000003.11:g.133 72532_13372533ins2 54	GRCh37.p13	First Pass	NC_000003.11	Chr3	13,372,532	13,372,532

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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