A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758797



Internal ID15706067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120459143..120469022hg38UCSC Ensembl
Innerchr10:122218655..122228534hg19UCSC Ensembl
Innerchr10:122208645..122218524hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg389880
hg199880
hg189880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552217
Supporting Variants
Samples
Known GenesPPAPDC1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv758797
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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