A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552029



Internal ID16339438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98523394..99122064hg38UCSC Ensembl
Innerchr10:100283151..100881821hg19UCSC Ensembl
Innerchr10:100273141..100871811hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38598671
hg19598671
hg18598671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1370n54
Supporting Variantsnssv756037
Samples
Known GenesHPSE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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