A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528421



Internal ID15455714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36065003..36066645hg38UCSC Ensembl
Innerchr14:36534209..36535851hg19UCSC Ensembl
Innerchr14:35603960..35605602hg18UCSC Ensembl
Innerchr14:35603960..35605602hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381643
hg191643
hg181643
hg171643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705013
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528421
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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