A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060564



Internal ID18803095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54819187..54867197hg38UCSC Ensembl
Innerchr19:55330642..55378652hg19UCSC Ensembl
Innerchr19:60022454..60070464hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3848011
hg1948011
hg1848011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3677n100
Supporting Variantsnssv3570415
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)nsv1060564
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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