A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825765



Internal ID15773035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35657915..35784870hg38UCSC Ensembl
Innerchr14:36127121..36254076hg19UCSC Ensembl
Innerchr14:35196872..35323827hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38126956
hg19126956
hg18126956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564342
Supporting Variants
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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