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dbVar

Database of genomic structural variation

nsv5964970

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: 144 SVs from 24 studies. See in: genome view

Submitted genomic12,168,313-12,168,313

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5964970	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	12,168,313	12,168,313
nsv5964970	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	12,168,546	12,168,546

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17409739	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17409739	Submitted genomic		NC_000006.12:g.121 68313_12168314ins5 0	GRCh38 (hg38)		NC_000006.12	Chr6	12,168,313	12,168,313
nssv17409739	Remapped	Perfect	NC_000006.11:g.121 68546_12168547ins5 0	GRCh37.p13	First Pass	NC_000006.11	Chr6	12,168,546	12,168,546

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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