A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521687



Internal ID15448980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28646910..28649036hg38UCSC Ensembl
Innerchr14:29116116..29118242hg19UCSC Ensembl
Innerchr14:28185867..28187993hg18UCSC Ensembl
Innerchr14:28185867..28187993hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382127
hg192127
hg182127
hg172127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698307
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521687
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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