A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525404



Internal ID15452697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93839821..93861128hg38UCSC Ensembl
Innerchr14:94306167..94327474hg19UCSC Ensembl
Innerchr14:93375920..93397227hg18UCSC Ensembl
Innerchr14:93375920..93397227hg17UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3821308
hg1921308
hg1821308
hg1721308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701528
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525404
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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