A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610528



Internal ID16397937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15462428..15476182hg38UCSC Ensembl
Innerchr8:15319937..15333691hg19UCSC Ensembl
Innerchr8:15364308..15378062hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3813755
hg1913755
hg1813755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12012n54
Supporting Variantsnssv1106861
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610528
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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