A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549981



Internal ID15990704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014587..13016863hg38UCSC Ensembl
Innerchr10:13056587..13058863hg19UCSC Ensembl
Innerchr10:13096593..13098869hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382277
hg192277
hg182277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958n54
Supporting Variantsnssv744018
Samples
Known GenesCCDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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