A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524648



Internal ID15451941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25141471..25146982hg38UCSC Ensembl
Innerchr14:25610677..25616188hg19UCSC Ensembl
Innerchr14:24680517..24686028hg18UCSC Ensembl
Innerchr14:24680517..24686028hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg385512
hg195512
hg185512
hg175512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700614
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524648
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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