A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580513



Internal ID18878794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89933859..90282526hg38UCSC Ensembl
Innerchr2:89972669..90321385hg19UCSC Ensembl
Innerchr2:89609974..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38348668
hg19348717
hg18348717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011499
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580513
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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