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dbVar

Database of genomic structural variation

nsv5926453

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:280

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

Submitted genomic127,957,321-127,957,600

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5926453	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	127,957,321	127,957,600
nsv5926453	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	128,969,567	128,969,846

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17448251	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17448251	Submitted genomic		NC_000008.11:g.127 957321_127957600de l	GRCh38 (hg38)		NC_000008.11	Chr8	127,957,321	127,957,600
nssv17448251	Remapped	Perfect	NC_000008.10:g.128 969567_128969846de l	GRCh37.p13	First Pass	NC_000008.10	Chr8	128,969,567	128,969,846

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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