A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013239



Internal ID19102457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26491082..26546950hg38UCSC Ensembl
Innerchr3:26532573..26588441hg19UCSC Ensembl
Innerchr3:26507577..26563445hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3855869
hg1955869
hg1855869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4710n100
Supporting Variantsnssv3589544
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)nsv1013239
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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