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dbVar

Database of genomic structural variation

nsv5920055

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:3,963

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: 384 SVs from 62 studies. See in: genome view

Submitted genomic42,332,913-42,336,875

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5920055	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	42,332,913	42,336,875
nsv5920055	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	42,190,431	42,194,393

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17443867	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17443867	Submitted genomic		NC_000008.11:g.423 32913_42336875del	GRCh38 (hg38)		NC_000008.11	Chr8	42,332,913	42,336,875
nssv17443867	Remapped	Perfect	NC_000008.10:g.421 90431_42194393del	GRCh37.p13	First Pass	NC_000008.10	Chr8	42,190,431	42,194,393

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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