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dbVar

Database of genomic structural variation

nsv5608468

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: 160 SVs from 27 studies. See in: genome view

Submitted genomic61,963,267-61,963,267

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5608468	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	61,963,267	61,963,267
nsv5608468	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	62,190,402	62,190,402

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17113354	insertion	SAMN00007882	Sequencing	Sequence alignment	1,354

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17113354	Submitted genomic		NC_000002.12:g.619 63267_61963268ins9 6	GRCh38 (hg38)		NC_000002.12	Chr2	61,963,267	61,963,267
nssv17113354	Remapped	Perfect	NC_000002.11:g.621 90402_62190403ins9 6	GRCh37.p13	First Pass	NC_000002.11	Chr2	62,190,402	62,190,402

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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