A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2771932



Internal ID15344592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70688910..70688966hg38UCSC Ensembl
Innerchr10:72448666..72448722hg19UCSC Ensembl
Innerchr10:72118672..72118728hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514572
Supporting Variants
SamplesNA18853
Known GenesADAMTS14
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2771932
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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