A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580242



Internal ID18531837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114622806..114643410hg38UCSC Ensembl
Innerchr2:115380383..115400987hg19UCSC Ensembl
Innerchr2:115096853..115117457hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3820605
hg1920605
hg1820605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006645
Supporting Variants
Samples
Known GenesDPP10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580242
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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