A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019960



Internal ID19109179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85313518..85426948hg38UCSC Ensembl
Innerchr6:86023236..86136666hg19UCSC Ensembl
Innerchr6:86079955..86193385hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38113431
hg19113431
hg18113431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648894
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)nsv1019960
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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