A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2811143



Internal ID15796357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20444997..20504803hg38UCSC Ensembl
Innerchr15:20650250..20710056hg19UCSC Ensembl
Innerchr15:18910264..18970070hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3859807
hg1959807
hg1859807
Variant TypeCNV gain
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514763
Supporting Variants
SamplesNA21479
Known GenesHERC2P3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2811143
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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