A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829170



Internal ID16123126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73062379..73080022hg38UCSC Ensembl
Innerchr14:73529087..73546730hg19UCSC Ensembl
Innerchr14:72598840..72616483hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3817644
hg1917644
hg1817644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565072
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)nssv829170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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