A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746562



Internal ID18698157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111079513..111107204hg38UCSC Ensembl
Innerchr5:110415211..110442903hg19UCSC Ensembl
Innerchr5:110443110..110470802hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3827692
hg1927693
hg1827693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023278
Supporting Variants
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)nssv3746562
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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