A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863017



Internal ID15810287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88575528hg38UCSC Ensembl
Innerchr16:88638854..88641936hg19UCSC Ensembl
Innerchr16:87166355..87169437hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383083
hg193083
hg183083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573665
Supporting Variants
Samples
Known GenesZC3H18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863017
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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