A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032342



Internal ID18774876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111083986..111107582hg38UCSC Ensembl
Innerchr5:110419684..110443281hg19UCSC Ensembl
Innerchr5:110447583..110471180hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3823597
hg1923598
hg1823598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5781n100
Supporting Variantsnssv3647041, nssv3647042, nssv3647044, nssv3746580, nssv3746579, nssv3647043, nssv3746577, nssv3746578
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)nsv1032342
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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