A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013305



Internal ID19102523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11883909..11912460hg38UCSC Ensembl
Innerchr3:11925383..11953934hg19UCSC Ensembl
Innerchr3:11900383..11928934hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3828552
hg1928552
hg1828552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4682n100
Supporting Variantsnssv3591957, nssv3591954, nssv3591956, nssv3591955
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)nsv1013305
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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