A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653159



Internal ID15389811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54247206hg38UCSC Ensembl
Innerchr19:54731679..54751065hg19UCSC Ensembl
Innerchr19:59423491..59442877hg18UCSC Ensembl
Innerchr19:59423491..59442877hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819402
hg1919387
hg1819387
hg1719387
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517129
Supporting Variants
Samples
Known GenesLILRA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653159
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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