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dbVar

Database of genomic structural variation

nsv5654432

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: 116 SVs from 30 studies. See in: genome view

Submitted genomic67,396,241-67,396,241

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5654432	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	67,396,241	67,396,241
nsv5654432	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	67,862,958	67,862,958

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17096728	insertion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17096728	Submitted genomic		NC_000014.9:g.6739 6241_67396242ins32 58	GRCh38 (hg38)		NC_000014.9	Chr14	67,396,241	67,396,241
nssv17096728	Remapped	Perfect	NC_000014.8:g.6786 2958_67862959ins32 58	GRCh37.p13	First Pass	NC_000014.8	Chr14	67,862,958	67,862,958

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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