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dbVar

Database of genomic structural variation

nsv6289766

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: 84 SVs from 22 studies. See in: genome view

Submitted genomic26,060,912-26,060,912

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6289766	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	26,060,912	26,060,912
nsv6289766	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	26,456,878	26,456,878

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17941294	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17941294	Submitted genomic		NC_000022.11:g.260 60912_26060913ins6 1	GRCh38 (hg38)		NC_000022.11	Chr22	26,060,912	26,060,912
nssv17941294	Remapped	Perfect	NC_000022.10:g.264 56878_26456879ins6 1	GRCh37.p13	First Pass	NC_000022.10	Chr22	26,456,878	26,456,878

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)
nssv17941294	0.041	80	1936

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