A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591966



Internal ID18890247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11895928..11920384hg38UCSC Ensembl
Innerchr3:11937402..11961858hg19UCSC Ensembl
Innerchr3:11912402..11936858hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3824457
hg1924457
hg1824457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001483
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)nssv3591966
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