A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033161



Internal ID19122383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25660633..25726587hg38UCSC Ensembl
Innerchr8:25518149..25584103hg19UCSC Ensembl
Innerchr8:25574066..25640020hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3865955
hg1965955
hg1865955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685508
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)nsv1033161
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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