A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864002



Internal ID15811272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907698..89908560hg38UCSC Ensembl
Innerchr16:89974106..89974968hg19UCSC Ensembl
Innerchr16:88501607..88502469hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38863
hg19863
hg18863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573834
Supporting Variants
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv864002
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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