A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527549



Internal ID15454842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86350817..86354861hg38UCSC Ensembl
Innerchr14:86817161..86821205hg19UCSC Ensembl
Innerchr14:85886914..85890958hg18UCSC Ensembl
Innerchr14:85886914..85890958hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg384045
hg194045
hg184045
hg174045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704010
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527549
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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