A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714976



Internal ID18666571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43166264..43214467hg38UCSC Ensembl
Innerchr13:43740400..43788603hg19UCSC Ensembl
Innerchr13:42638400..42686603hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3848204
hg1948204
hg1848204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042786
Supporting Variants
Samples
Known GenesENOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714976
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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