A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859075



Internal ID15806345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68816880..68972894hg38UCSC Ensembl
Innerchr16:68850783..69006797hg19UCSC Ensembl
Innerchr16:67408284..67564298hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38156015
hg19156015
hg18156015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572910
Supporting Variants
Samples
Known GenesCDH1, TANGO6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859075
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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