A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015792



Internal ID18758326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34774140..34919539hg38UCSC Ensembl
Innerchr6:34741917..34887316hg19UCSC Ensembl
Innerchr6:34849895..34995294hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38145400
hg19145400
hg18145400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5955n100
Supporting Variantsnssv3657371
Samples
Known GenesANKS1A, TAF11, UHRF1BP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015792
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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