A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647026



Internal ID18598621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111069619..111103025hg38UCSC Ensembl
Innerchr5:110405317..110438724hg19UCSC Ensembl
Innerchr5:110433216..110466623hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3833407
hg1933408
hg1833408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032351
Supporting Variants
Samples
Known GenesTSLP, WDR36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3647026
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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