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dbVar

Database of genomic structural variation

nsv6212211

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: 109 SVs from 30 studies. See in: genome view

Submitted genomic37,611,748-37,611,748

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6212211	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	37,611,748	37,611,748
nsv6212211	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	38,077,349	38,077,349

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17875769	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17875769	Submitted genomic		NC_000001.11:g.376 11748_37611749ins7 1	GRCh38 (hg38)		NC_000001.11	Chr1	37,611,748	37,611,748
nssv17875769	Remapped	Perfect	NC_000001.10:g.380 77349_38077350ins7 1	GRCh37.p13	First Pass	NC_000001.10	Chr1	38,077,349	38,077,349

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)
nssv17875769	0.102	189	1860

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