A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933813



Internal ID16227769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239400622..239401522hg38UCSC Ensembl
Innerchr2:240322316..240323216hg19UCSC Ensembl
Innerchr2:239987253..239988153hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584791
Supporting Variants
Samples
Known GenesHDAC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933813
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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