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dbVar

Database of genomic structural variation

nsv5659795

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: 95 SVs from 33 studies. See in: genome view

Submitted genomic96,311,584-96,311,584

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659795	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	96,311,584	96,311,584
nsv5659795	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	96,705,362	96,705,362

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17092422	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17092422	Submitted genomic		NC_000012.12:g.963 11584_96311585ins3 21	GRCh38 (hg38)		NC_000012.12	Chr12	96,311,584	96,311,584
nssv17092422	Remapped	Perfect	NC_000012.11:g.967 05362_96705363ins3 21	GRCh37.p13	First Pass	NC_000012.11	Chr12	96,705,362	96,705,362

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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