A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2878741



Internal ID15734804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:230699809..230701265hg38UCSC Ensembl
Innerchr2:231564524..231565980hg19UCSC Ensembl
Innerchr2:231272768..231274224hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381457
hg191457
hg181457
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514124
Supporting Variants
SamplesNA19118
Known GenesLOC151475
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2878741
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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