A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565065



Internal ID16352474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73062077..73079919hg38UCSC Ensembl
Innerchr14:73528785..73546627hg19UCSC Ensembl
Innerchr14:72598538..72616380hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3817843
hg1917843
hg1817843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3754n54
Supporting Variantsnssv829140
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565065
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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