A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525018



Internal ID15452311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:59064275..59076020hg38UCSC Ensembl
Innerchr8:59976834..59988579hg19UCSC Ensembl
Innerchr8:60139388..60151133hg18UCSC Ensembl
Innerchr8:60139388..60151133hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3811746
hg1911746
hg1811746
hg1711746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701057
Samples
Known GenesTOX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525018
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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