A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038623



Internal ID19127842
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 StatusM
Merged Variants
Supporting Variantsnssv3531222
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)nsv1038623
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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