A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528333



Internal ID15455626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34383535..34517816hg38UCSC Ensembl
Innerchr10:34672463..34806744hg19UCSC Ensembl
Innerchr10:34712469..34846750hg18UCSC Ensembl
Innerchr10:34712469..34846750hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38134282
hg19134282
hg18134282
hg17134282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704915
Samples
Known GenesPARD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528333
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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