A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552323



Internal ID16339732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130702291..130750902hg38UCSC Ensembl
Innerchr10:132500555..132549166hg19UCSC Ensembl
Innerchr10:132390545..132439156hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3848612
hg1948612
hg1848612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv760804
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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