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dbVar

Database of genomic structural variation

nsv5612212

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: 886 SVs from 63 studies. See in: genome view

Submitted genomic1,289,395-1,289,395

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5612212	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	1,289,395	1,289,395
nsv5612212	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	1,224,775	1,224,775

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060396	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
nssv17060396	Submitted genomic		NC_000001.11:g.128 9395_1289396ins107	GRCh38 (hg38)		NC_000001.11	Chr1	1,289,395	1,289,395
nssv17060396	Remapped	Perfect	NC_000001.10:g.122 4775_1224776ins107	GRCh37.p13	First Pass	NC_000001.10	Chr1	1,224,775	1,224,775

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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