A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018716



Internal ID18761249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31394533..31513522hg38UCSC Ensembl
Innerchr6:31362310..31481299hg19UCSC Ensembl
Innerchr6:31470289..31589278hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38118990
hg19118990
hg18118990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5942n100
Supporting Variantsnssv3655881
Samples
Known GenesHCG26, HCP5, MICA, MICB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018716
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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