A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585678



Internal ID18883959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:214590564..214631740hg38UCSC Ensembl
Innerchr2:215455288..215496464hg19UCSC Ensembl
Innerchr2:215163533..215204709hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3841177
hg1941177
hg1841177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008188
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)nssv3585678
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