A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048064



Internal ID19137283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68524324..68546049hg38UCSC Ensembl
Innerchr14:68991041..69012766hg19UCSC Ensembl
Innerchr14:68060794..68082519hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3821726
hg1921726
hg1821726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531107
Samples
Known GenesRAD51B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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