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dbVar

Database of genomic structural variation

nsv5870236

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:78

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: 173 SVs from 30 studies. See in: genome view

Submitted genomic190,166,644-190,166,721

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5870236	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	190,166,644	190,166,721
nsv5870236	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	190,135,774	190,135,851

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17351167	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17351167	Submitted genomic		NC_000001.11:g.190 166644_190166721de l	GRCh38 (hg38)		NC_000001.11	Chr1	190,166,644	190,166,721
nssv17351167	Remapped	Perfect	NC_000001.10:g.190 135774_190135851de l	GRCh37.p13	First Pass	NC_000001.10	Chr1	190,135,774	190,135,851

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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