A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612409



Internal ID16399818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136865099hg38UCSC Ensembl
Innerchr8:137687955..137877342hg19UCSC Ensembl
Innerchr8:137757137..137946524hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38189388
hg19189388
hg18189388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122358, nssv1122357, nssv1122356
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612409
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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