A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528115



Internal ID15108722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1714246..1732370hg38UCSC Ensembl
Innerchr10:1756440..1774564hg19UCSC Ensembl
Innerchr10:1746440..1764564hg18UCSC Ensembl
Innerchr10:1746440..1764564hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3818125
hg1918125
hg1818125
hg1718125
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704658
Samples
Known GenesADARB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528115
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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