A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv759461



Internal ID16053417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120467435..120469022hg38UCSC Ensembl
Innerchr10:122226947..122228534hg19UCSC Ensembl
Innerchr10:122216937..122218524hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg381588
hg191588
hg181588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552221
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)nssv759461
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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