A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523667



Internal ID15450960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31956023..31985166hg38UCSC Ensembl
Innerchr14:32425229..32454372hg19UCSC Ensembl
Innerchr14:31494980..31524123hg18UCSC Ensembl
Innerchr14:31494980..31524123hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3829144
hg1929144
hg1829144
hg1729144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699469
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523667
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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