A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549979



Internal ID15990702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014587..13015403hg38UCSC Ensembl
Innerchr10:13056587..13057403hg19UCSC Ensembl
Innerchr10:13096593..13097409hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38817
hg19817
hg18817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744016
Samples
Known GenesCCDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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