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dbVar

Database of genomic structural variation

nsv5948002

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: 141 SVs from 35 studies. See in: genome view

Submitted genomic71,179,624-71,179,624

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5948002	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	71,179,624	71,179,624
nsv5948002	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	70,644,610	70,644,610

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17431152	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17431152	Submitted genomic		NC_000007.14:g.711 79624_71179625ins2 25	GRCh38 (hg38)		NC_000007.14	Chr7	71,179,624	71,179,624
nssv17431152	Remapped	Perfect	NC_000007.13:g.706 44610_70644611ins2 25	GRCh37.p13	First Pass	NC_000007.13	Chr7	70,644,610	70,644,610

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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