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dbVar

Database of genomic structural variation

nsv5951226

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 111 SVs from 22 studies. See in: genome view

Submitted genomic36,429,253-36,429,253

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5951226	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	36,429,253	36,429,253
nsv5951226	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	36,397,030	36,397,030

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17430548	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17430548	Submitted genomic		NC_000006.12:g.364 29253_36429254ins4 01	GRCh38 (hg38)		NC_000006.12	Chr6	36,429,253	36,429,253
nssv17430548	Remapped	Perfect	NC_000006.11:g.363 97030_36397031ins4 01	GRCh37.p13	First Pass	NC_000006.11	Chr6	36,397,030	36,397,030

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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