A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855502



Internal ID16149458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31209256..31214084hg38UCSC Ensembl
Innerchr16:31220577..31225405hg19UCSC Ensembl
Innerchr16:31128078..31132906hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384829
hg194829
hg184829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571824
Supporting Variants
Samples
Known GenesTRIM72
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855502
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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