A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3581609



Internal ID18879890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45106843..45124910hg38UCSC Ensembl
Innerchr2:45333982..45352049hg19UCSC Ensembl
Innerchr2:45187486..45205553hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3818068
hg1918068
hg1818068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997810
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)nssv3581609
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