A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017861



Internal ID19107078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:5921245..6170419hg38UCSC Ensembl
Innerchr8:5778767..6027940hg19UCSC Ensembl
Innerchr8:5766175..6015348hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38249175
hg19249174
hg18249174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6863n100
Supporting Variantsnssv3753953
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)nsv1017861
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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