A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033252



Internal ID19122474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37482631..37569366hg38UCSC Ensembl
Innerchr8:37340149..37426884hg19UCSC Ensembl
Innerchr8:37459307..37546042hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3886736
hg1986736
hg1886736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685569
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)nsv1033252
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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