A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031161



Internal ID18773694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46007639..46831628hg38UCSC Ensembl
Innerchr8:46919261..47743250hg19UCSC Ensembl
Innerchr8:47038426..47862415hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38823990
hg19823990
hg18823990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7202n100
Supporting Variantsnssv3687397
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)nsv1031161
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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