A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829187



Internal ID16123143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73063508..73080022hg38UCSC Ensembl
Innerchr14:73530216..73546730hg19UCSC Ensembl
Innerchr14:72599969..72616483hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3816515
hg1916515
hg1816515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565085
Supporting Variants
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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