A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520403



Internal ID15447696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:115115219..115116965hg38UCSC Ensembl
Innerchr2:115872796..115874542hg19UCSC Ensembl
Innerchr2:115589266..115591012hg18UCSC Ensembl
Innerchr2:115589026..115590772hg17UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381747
hg191747
hg181747
hg171747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697395
Samples
Known GenesDPP10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520403
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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