A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523136



Internal ID18474731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21319810..21353356hg38UCSC Ensembl
Innerchr13:21893949..21927495hg19UCSC Ensembl
Innerchr13:20791949..20825495hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3833547
hg1933547
hg1833547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047558
Supporting Variants
Samples
Known GenesLINC00539, MIPEPP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523136
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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