A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589539



Internal ID18887820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26297590..26392621hg38UCSC Ensembl
Innerchr3:26339081..26434112hg19UCSC Ensembl
Innerchr3:26314085..26409116hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3895032
hg1995032
hg1895032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001468
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)nssv3589539
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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