A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026217



Internal ID18768749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111080525..111105496hg38UCSC Ensembl
Innerchr5:110416223..110441195hg19UCSC Ensembl
Innerchr5:110444122..110469094hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3824972
hg1924973
hg1824973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5781n100
Supporting Variantsnssv3746565
Samples
Known GenesWDR36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026217
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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