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dbVar

Database of genomic structural variation

nsv5956788

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: 142 SVs from 37 studies. See in: genome view

Submitted genomic26,947,257-26,947,257

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5956788	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	26,947,257	26,947,257
nsv5956788	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	26,915,036	26,915,036

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17432533	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17432533	Submitted genomic		NC_000006.12:g.269 47257_26947258ins1 74	GRCh38 (hg38)		NC_000006.12	Chr6	26,947,257	26,947,257
nssv17432533	Remapped	Perfect	NC_000006.11:g.269 15036_26915037ins1 74	GRCh37.p13	First Pass	NC_000006.11	Chr6	26,915,036	26,915,036

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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