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dbVar

Database of genomic structural variation

nsv6227616

Organism: Homo sapiens

Study:nstd214 (Naslavsky et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Naslavsky 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: 86 SVs from 18 studies. See in: genome view

Submitted genomic10,762,833-10,762,833

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6227616	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	10,762,833	10,762,833
nsv6227616	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	10,856,690	10,856,690

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17933760	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17933760	Submitted genomic		NC_000016.10:g.107 62833_10762834ins7 0	GRCh38 (hg38)		NC_000016.10	Chr16	10,762,833	10,762,833
nssv17933760	Remapped	Perfect	NC_000016.9:g.1085 6690_10856691ins70	GRCh37.p13	First Pass	NC_000016.9	Chr16	10,856,690	10,856,690

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)
nssv17933760	<0.001	1	2332

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