A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573718



Internal ID16014441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88807259..88810716hg38UCSC Ensembl
Innerchr16:88873667..88877124hg19UCSC Ensembl
Innerchr16:87401168..87404625hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg383458
hg193458
hg183458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863302
Samples
Known GenesAPRT, CDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573718
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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