A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863702



Internal ID15810972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89907389..89908454hg38UCSC Ensembl
Innerchr16:89973797..89974862hg19UCSC Ensembl
Innerchr16:88501298..88502363hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381066
hg191066
hg181066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573816
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)nssv863702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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