A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021739



Internal ID18764273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111083986..111119568hg38UCSC Ensembl
Innerchr5:110419684..110455266hg19UCSC Ensembl
Innerchr5:110447583..110483165hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3835583
hg1935583
hg1835583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5780n100
Supporting Variantsnssv3647045
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)nsv1021739
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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