A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527185



Internal ID15454478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101580299..101608897hg38UCSC Ensembl
Innerchr10:103340056..103368654hg19UCSC Ensembl
Innerchr10:103330046..103358644hg18UCSC Ensembl
Innerchr10:103330046..103358644hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3828599
hg1928599
hg1828599
hg1728599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703581
Samples
Known GenesDPCD, MIR3158-1, MIR3158-2, POLL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527185
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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