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dbVar

Database of genomic structural variation

nsv5660571

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: 223 SVs from 31 studies. See in: genome view

Submitted genomic1,605,014-1,605,014

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660571	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	1,605,014	1,605,014
nsv5660571	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	1,714,180	1,714,180

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17078780	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17078780	Submitted genomic		NC_000012.12:g.160 5014_1605015ins398	GRCh38 (hg38)		NC_000012.12	Chr12	1,605,014	1,605,014
nssv17078780	Remapped	Perfect	NC_000012.11:g.171 4180_1714181ins398	GRCh37.p13	First Pass	NC_000012.11	Chr12	1,714,180	1,714,180

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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