A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861949



Internal ID15809219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82151715..83457169hg38UCSC Ensembl
Innerchr16:82185320..83490774hg19UCSC Ensembl
Innerchr16:80742821..82048275hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381305455
hg191305455
hg181305455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573373
Supporting Variants
Samples
Known GenesCDH13, MIR8058, MPHOSPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861949
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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