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dbVar

Database of genomic structural variation

nsv5287579

Organism: Homo sapiens

Study:nstd204 (Chen et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:324,700

Publication(s):Chen et al. 2021

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: 1384 SVs from 82 studies. See in: genome view

Submitted genomic36,469,001-36,793,700

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5287579	Submitted genomic		GRCh38.p13	Primary Assembly		NC_000019.10	Chr19	36,469,001	36,793,700
nsv5287579	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	36,959,903	37,284,602

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16825108	copy number variation	Sequencing	Read depth

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16825108	Submitted genomic		GRCh38.p13		NC_000019.10	Chr19	36,469,001	36,793,700
nssv16825108	Remapped	Perfect	GRCh37.p13	First Pass	NC_000019.9	Chr19	36,959,903	37,284,602

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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