A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573712



Internal ID16014435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88796728..88809084hg38UCSC Ensembl
Innerchr16:88863136..88875492hg19UCSC Ensembl
Innerchr16:87390637..87402993hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3812357
hg1912357
hg1812357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863297
Samples
Known GenesCDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573712
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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