A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2926185



Internal ID15622602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160598642..160650482hg38UCSC Ensembl
Innerchr6:161019674..161071514hg19UCSC Ensembl
Innerchr6:160939664..160991504hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3851841
hg1951841
hg1851841
Variant TypeCNV gain
Copy Number37
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515029
Supporting Variants
SamplesNA12146
Known GenesLPA
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2926185
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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