A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065329



Internal ID18807860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54819187..54868123hg38UCSC Ensembl
Innerchr19:55330642..55379578hg19UCSC Ensembl
Innerchr19:60022454..60071390hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3848937
hg1948937
hg1848937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3677n100
Supporting Variantsnssv3726643
Samples
Known GenesKIR2DS4, KIR3DL1, KIR3DL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065329
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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