A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2778125



Internal ID15248272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014874..13017110hg38UCSC Ensembl
Innerchr10:13056874..13059110hg19UCSC Ensembl
Innerchr10:13096880..13099116hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382237
hg192237
hg182237
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514543
Supporting Variants
SamplesNA07056
Known GenesCCDC3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2778125
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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