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dbVar

Database of genomic structural variation

nsv5970579

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

Submitted genomic32,846,745-32,846,745

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5970579	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	32,846,745	32,846,745
nsv5970579	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	32,999,679	32,999,679

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17366660	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17366660	Submitted genomic		NC_000012.12:g.328 46745_32846746ins1 79	GRCh38 (hg38)		NC_000012.12	Chr12	32,846,745	32,846,745
nssv17366660	Remapped	Perfect	NC_000012.11:g.329 99679_32999680ins1 79	GRCh37.p13	First Pass	NC_000012.11	Chr12	32,999,679	32,999,679

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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