A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv863339



Internal ID15810609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89647834..89648410hg38UCSC Ensembl
Innerchr16:89714242..89714818hg19UCSC Ensembl
Innerchr16:88241743..88242319hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38577
hg19577
hg18577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573742
Supporting Variants
Samples
Known GenesCHMP1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv863339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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