A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681766



Internal ID15071732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54714899..54866553hg38UCSC Ensembl
Innerchr19:55226402..55378008hg19UCSC Ensembl
Innerchr19:59918214..60069820hg18UCSC Ensembl
Innerchr19:59918214..60069820hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38151655
hg19151607
hg18151607
hg17151607
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517143
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, KIR3DL3, LOC100287534
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681766
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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