A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817439



Internal ID16111395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91347886..91349218hg38UCSC Ensembl
Innerchr13:92000140..92001472hg19UCSC Ensembl
Innerchr13:90798141..90799473hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381333
hg191333
hg181333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562704
Supporting Variants
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817439
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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