A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv857553



Internal ID16151509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55762760..55793775hg38UCSC Ensembl
Innerchr16:55796672..55827687hg19UCSC Ensembl
Innerchr16:54354173..54385188hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3831016
hg1931016
hg1831016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572652
Supporting Variants
Samples
Known GenesCES1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv857553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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