A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026924



Internal ID19116142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25133577..25154738hg38UCSC Ensembl
Innerchr8:24991092..25012253hg19UCSC Ensembl
Innerchr8:25047009..25068170hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3821162
hg1921162
hg1821162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685493
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)nsv1026924
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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