A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692313



Internal ID15428965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50757732..50760253hg38UCSC Ensembl
Innerchr19:51260989..51263510hg19UCSC Ensembl
Innerchr19:55952801..55955322hg18UCSC Ensembl
Innerchr19:55952801..55955322hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382522
hg192522
hg182522
hg172522
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517376
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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