A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525823



Internal ID15453116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81753206..81801601hg38UCSC Ensembl
Innerchr14:82219550..82267945hg19UCSC Ensembl
Innerchr14:81289303..81337698hg18UCSC Ensembl
Innerchr14:81289303..81337698hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3848396
hg1948396
hg1848396
hg1748396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702011
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525823
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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