A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528996



Internal ID15456289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21752285..21774090hg38UCSC Ensembl
Innerchr14:22220569..22242293hg19UCSC Ensembl
Innerchr14:21290409..21312133hg18UCSC Ensembl
Innerchr14:21290409..21312133hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3821806
hg1921725
hg1821725
hg1721725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705700
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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