A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516289



Internal ID15443582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26614451..26620276hg38UCSC Ensembl
Innerchr14:27083657..27089482hg19UCSC Ensembl
Innerchr14:26153497..26159322hg18UCSC Ensembl
Innerchr14:26153497..26159322hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385826
hg195826
hg185826
hg175826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688878, nssv679872, nssv674303, nssv667362
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516289
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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