A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565069



Internal ID16352478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73062077..73082147hg38UCSC Ensembl
Innerchr14:73528785..73548855hg19UCSC Ensembl
Innerchr14:72598538..72618608hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3820071
hg1920071
hg1820071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3754n54
Supporting Variantsnssv829165, nssv829166
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565069
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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