A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026368



Internal ID19115586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15026899..15063559hg38UCSC Ensembl
Innerchr6:15027130..15063790hg19UCSC Ensembl
Innerchr6:15135109..15171769hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3836661
hg1936661
hg1836661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5919n100
Supporting Variantsnssv3654794
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)nsv1026368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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