A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025666



Internal ID19114884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115039025..115137278hg38UCSC Ensembl
Innerchr8:116051254..116149507hg19UCSC Ensembl
Innerchr8:116120430..116218683hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3898254
hg1998254
hg1898254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7299n100
Supporting Variantsnssv3691452
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)nsv1025666
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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