A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024962



Internal ID19114180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7425013..7452602hg38UCSC Ensembl
Innerchr6:7425246..7452835hg19UCSC Ensembl
Innerchr6:7370245..7397834hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3827590
hg1927590
hg1827590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5914n100
Supporting Variantsnssv3654748
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)nsv1024962
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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