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dbVar

Database of genomic structural variation

nsv5625272

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: 211 SVs from 34 studies. See in: genome view

Submitted genomic143,040,660-143,040,660

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5625272	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	143,040,660	143,040,660
nsv5625272	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	144,122,077	144,122,077

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17144727	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
nssv17144727	Submitted genomic		NC_000008.11:g.143 040660_143040661in s51	GRCh38 (hg38)		NC_000008.11	Chr8	143,040,660	143,040,660
nssv17144727	Remapped	Perfect	NC_000008.10:g.144 122077_144122078in s51	GRCh37.p13	First Pass	NC_000008.10	Chr8	144,122,077	144,122,077

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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