A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660076



Internal ID15050042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42954411..43035037hg38UCSC Ensembl
Innerchr19:43458563..43539189hg19UCSC Ensembl
Innerchr19:48150403..48231029hg18UCSC Ensembl
Innerchr19:48150403..48231029hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3880627
hg1980627
hg1880627
hg1780627
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660076
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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