A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032148



Internal ID19121370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134873781..135011708hg38UCSC Ensembl
Innerchr8:135886024..136023951hg19UCSC Ensembl
Innerchr8:135955206..136093133hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38137928
hg19137928
hg18137928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692719
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)nsv1032148
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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