A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565051



Internal ID16352460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73047155..73064831hg38UCSC Ensembl
Innerchr14:73513863..73531539hg19UCSC Ensembl
Innerchr14:72583616..72601292hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3817677
hg1917677
hg1817677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829097
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565051
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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