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dbVar

Database of genomic structural variation

nsv5961197

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 130 SVs from 28 studies. See in: genome view

Submitted genomic12,623,474-12,623,474

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961197	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	12,623,474	12,623,474
nsv5961197	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	12,665,473	12,665,473

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17360569	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17360569	Submitted genomic		NC_000010.11:g.126 23474_12623475ins5 6	GRCh38 (hg38)		NC_000010.11	Chr10	12,623,474	12,623,474
nssv17360569	Remapped	Perfect	NC_000010.10:g.126 65473_12665474ins5 6	GRCh37.p13	First Pass	NC_000010.10	Chr10	12,665,473	12,665,473

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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