A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592652



Internal ID16380061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181496039..181602608hg38UCSC Ensembl
Innerchr3:181213827..181320396hg19UCSC Ensembl
Innerchr3:182696521..182803090hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38106570
hg19106570
hg18106570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982548
Samples
Known GenesSOX2-OT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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