A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013204



Internal ID18755735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15761347..15834614hg38UCSC Ensembl
Innerchr4:15762970..15836237hg19UCSC Ensembl
Innerchr4:15372068..15445335hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3873268
hg1973268
hg1873268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5145n100
Supporting Variantsnssv3619843
Samples
Known GenesCD38
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013204
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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