A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013292



Internal ID19102510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65089543..65114617hg38UCSC Ensembl
Innerchr3:65075218..65100292hg19UCSC Ensembl
Innerchr3:65050258..65075332hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3825075
hg1925075
hg1825075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594612
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)nsv1013292
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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