A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088753



Internal ID21280792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32439762..32911564hg38UCSC Ensembl
Innerchr10:32728690..33200492hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38471803
hg19471803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117865
Supporting Variants
Samplessample302
Known GenesCCDC7, ITGB1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088753
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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