A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549980



Internal ID15990703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014587..13016556hg38UCSC Ensembl
Innerchr10:13056587..13058556hg19UCSC Ensembl
Innerchr10:13096593..13098562hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381970
hg191970
hg181970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958n54
Supporting Variantsnssv744017
Samples
Known GenesCCDC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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