A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2772059



Internal ID15324475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49800340..49906388hg38UCSC Ensembl
Innerchr10:51008386..51114434hg19UCSC Ensembl
Innerchr10:50678392..50784440hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38106049
hg19106049
hg18106049
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514557
Supporting Variants
SamplesNA18519
Known GenesPARG
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2772059
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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