A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686738



Internal ID15423390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54245159hg38UCSC Ensembl
Innerchr19:54731679..54749011hg19UCSC Ensembl
Innerchr19:59423491..59440823hg18UCSC Ensembl
Innerchr19:59423491..59440823hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817355
hg1917333
hg1817333
hg1717333
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)nssv686738
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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