A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016657



Internal ID19105874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134049828..134078529hg38UCSC Ensembl
Innerchr8:135062071..135090772hg19UCSC Ensembl
Innerchr8:135131253..135159954hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3828702
hg1928702
hg1828702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7324n100
Supporting Variantsnssv3691601
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)nsv1016657
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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