A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2932675



Internal ID15274604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31985264..31990776hg38UCSC Ensembl
Innerchr6:31953041..31958553hg19UCSC Ensembl
Innerchr6:32061020..32066532hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385513
hg195513
hg185513
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515035
Supporting Variants
SamplesNA12144
Known GenesC4A, C4B, C4B_2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2932675
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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