A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673401



Internal ID15410053
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 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)nssv673401
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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