A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679756



Internal ID15416408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54600262..54651887hg38UCSC Ensembl
Innerchr19:55111727..55163337hg19UCSC Ensembl
Innerchr19:59803539..59855149hg18UCSC Ensembl
Innerchr19:59803539..59855149hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3851626
hg1951611
hg1851611
hg1751611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516569
Supporting Variants
Samples
Known GenesLILRA1, LILRB1, MIR8061
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679756
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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