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dbVar

Database of genomic structural variation

nsv5623844

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: 130 SVs from 28 studies. See in: genome view

Submitted genomic145,826,765-145,826,765

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5623844	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	145,826,765	145,826,765
nsv5623844	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	146,747,917	146,747,917

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17135272	insertion	SAMN00249890	Sequencing	Sequence alignment	1,169

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17135272	Submitted genomic		NC_000004.12:g.145 826765_145826766in s51	GRCh38 (hg38)		NC_000004.12	Chr4	145,826,765	145,826,765
nssv17135272	Remapped	Perfect	NC_000004.11:g.146 747917_146747918in s51	GRCh37.p13	First Pass	NC_000004.11	Chr4	146,747,917	146,747,917

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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