A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639096



Internal ID18590691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80559891..80580410hg38UCSC Ensembl
Innerchr5:79855710..79876229hg19UCSC Ensembl
Innerchr5:79891466..79911985hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3820520
hg1920520
hg1820520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027663
Supporting Variants
Samples
Known GenesANKRD34B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639096
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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