A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528509



Internal ID15455802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28755627..28761654hg38UCSC Ensembl
Innerchr14:29224833..29230860hg19UCSC Ensembl
Innerchr14:28294584..28300611hg18UCSC Ensembl
Innerchr14:28294584..28300611hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg386028
hg196028
hg186028
hg176028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705116
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528509
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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