A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020967



Internal ID19110185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9071143..9669549hg38UCSC Ensembl
Innerchr6:9071376..9669782hg19UCSC Ensembl
Innerchr6:9016375..9777768hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38598407
hg19598407
hg18761394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654756
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)nsv1020967
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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