A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591953



Internal ID18890234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11883909..11912166hg38UCSC Ensembl
Innerchr3:11925383..11953640hg19UCSC Ensembl
Innerchr3:11900383..11928640hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3828258
hg1928258
hg1828258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014141
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)nssv3591953
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