A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656973



Internal ID15393625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54229182..54247206hg38UCSC Ensembl
Innerchr19:54733056..54751065hg19UCSC Ensembl
Innerchr19:59424868..59442877hg18UCSC Ensembl
Innerchr19:59424868..59442877hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3818025
hg1918010
hg1818010
hg1718010
Variant TypeCNV gain
Copy Number
Allele State
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)nssv656973
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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