A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519523



Internal ID15446816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41448023..41495302hg38UCSC Ensembl
Innerchr19:41953928..42001210hg19UCSC Ensembl
Innerchr19:46645768..46693050hg18UCSC Ensembl
Innerchr19:46645768..46693050hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3847280
hg1947283
hg1847283
hg1747283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656673, nssv671711, nssv659196
Samples
Known GenesLOC100505495
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519523
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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