A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863007



Internal ID15810277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88572446..88575358hg38UCSC Ensembl
Innerchr16:88638854..88641766hg19UCSC Ensembl
Innerchr16:87166355..87169267hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382913
hg192913
hg182913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573662
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)nssv863007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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