A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520139



Internal ID15100746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2910530..2913845hg38UCSC Ensembl
Innerchr3:2952214..2955529hg19UCSC Ensembl
Innerchr3:2927214..2930529hg18UCSC Ensembl
Innerchr3:2927214..2930529hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg383316
hg193316
hg183316
hg173316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681022, nssv661110
Samples
Known GenesCNTN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520139
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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