A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610800



Internal ID16398209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25115293..25134659hg38UCSC Ensembl
Innerchr8:24972808..24992174hg19UCSC Ensembl
Innerchr8:25028725..25048091hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3819367
hg1919367
hg1819367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12062n54
Supporting Variantsnssv1107809, nssv1107810, nssv1107807, nssv1107808
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610800
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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