A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041985



Internal ID18784516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77411078..77470626hg38UCSC Ensembl
Innerchr14:77877421..77936969hg19UCSC Ensembl
Innerchr14:76947174..77006722hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3859549
hg1959549
hg1859549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713529
Samples
Known GenesAHSA1, NOXRED1, VIPAS39
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041985
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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