A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829098



Internal ID16123054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73057833..73080138hg38UCSC Ensembl
Innerchr14:73524541..73546846hg19UCSC Ensembl
Innerchr14:72594294..72616599hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3822306
hg1922306
hg1822306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565052
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)nssv829098
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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