A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2899613



Internal ID15354231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46753234..46808734hg38UCSC Ensembl
Innerchr3:46794724..46850224hg19UCSC Ensembl
Innerchr3:46769728..46825228hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3855501
hg1955501
hg1855501
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514149
Supporting Variants
SamplesNA18908
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2899613
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer