A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669686



Internal ID15059652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43155365..43335936hg38UCSC Ensembl
Innerchr19:43659517..43840088hg19UCSC Ensembl
Innerchr19:48351357..48531928hg18UCSC Ensembl
Innerchr19:48351357..48531928hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38180572
hg19180572
hg18180572
hg17180572
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669686
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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