A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829186



Internal ID16123142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73063508..73079971hg38UCSC Ensembl
Innerchr14:73530216..73546679hg19UCSC Ensembl
Innerchr14:72599969..72616432hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3816464
hg1916464
hg1816464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565084
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)nssv829186
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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