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dbVar

Database of genomic structural variation

nsv5642916

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: 118 SVs from 20 studies. See in: genome view

Submitted genomic12,198,438-12,198,438

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5642916	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	12,198,438	12,198,438
nsv5642916	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	12,240,437	12,240,437

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17067593	insertion	SAMN00016965	Sequencing	Sequence alignment	1,475

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17067593	Submitted genomic		NC_000010.11:g.121 98438_12198439ins8 7	GRCh38 (hg38)		NC_000010.11	Chr10	12,198,438	12,198,438
nssv17067593	Remapped	Perfect	NC_000010.10:g.122 40437_12240438ins8 7	GRCh37.p13	First Pass	NC_000010.10	Chr10	12,240,437	12,240,437

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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