A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531222



Internal ID18829503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:79937301..80027968hg38UCSC Ensembl
Innerchr14:80403644..80494311hg19UCSC Ensembl
Innerchr14:79473397..79564064hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3890668
hg1990668
hg1890668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038623
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531222
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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