A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610878



Internal ID16398287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30313738..30336242hg38UCSC Ensembl
Innerchr8:30171254..30193758hg19UCSC Ensembl
Innerchr8:30290796..30313300hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822505
hg1922505
hg1822505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109446
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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