A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525498



Internal ID18823779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95284604..95380575hg38UCSC Ensembl
Innerchr13:95936858..96032829hg19UCSC Ensembl
Innerchr13:94734859..94830830hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3895972
hg1995972
hg1895972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044162
Supporting Variants
Samples
Known GenesABCC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525498
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