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dbVar

Database of genomic structural variation

nsv5952399

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: 113 SVs from 26 studies. See in: genome view

Submitted genomic87,407,647-87,407,647

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5952399	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	87,407,647	87,407,647
nsv5952399	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	88,117,365	88,117,365

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17433343	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17433343	Submitted genomic		NC_000006.12:g.874 07647_87407648ins4 81	GRCh38 (hg38)		NC_000006.12	Chr6	87,407,647	87,407,647
nssv17433343	Remapped	Perfect	NC_000006.11:g.881 17365_88117366ins4 81	GRCh37.p13	First Pass	NC_000006.11	Chr6	88,117,365	88,117,365

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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