A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610782



Internal ID16398191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:24247754..24278265hg38UCSC Ensembl
Innerchr8:24105267..24135778hg19UCSC Ensembl
Innerchr8:24161212..24191723hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3830512
hg1930512
hg1830512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12058n54
Supporting Variantsnssv1107484
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610782
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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