A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001468



Internal ID19090685
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 StatusM
Merged Variantsdgv4709n100
Supporting Variantsnssv3589539
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)nsv1001468
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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