A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856155



Internal ID16150111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34069624..34218490hg38UCSC Ensembl
Innerchr16:33872091..34020957hg19UCSC Ensembl
Innerchr16:33779592..33928458hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38148867
hg19148867
hg18148867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572331
Supporting Variants
Samples
Known GenesLINC00273
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv856155
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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