A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020835



Internal ID18763369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111082177..111107582hg38UCSC Ensembl
Innerchr5:110417875..110443281hg19UCSC Ensembl
Innerchr5:110445774..110471180hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3825406
hg1925407
hg1825407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5781n100
Supporting Variantsnssv3746575, nssv3647038, nssv3746576, nssv3746574
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)nsv1020835
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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