A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064703



Internal ID18807234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54736516..54822417hg38UCSC Ensembl
Innerchr19:55247983..55333872hg19UCSC Ensembl
Innerchr19:59939795..60025684hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3885902
hg1985890
hg1885890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3669n100
Supporting Variantsnssv3726580
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR3DL1, KIR3DL3, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064703
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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