A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612408



Internal ID16399817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136864159hg38UCSC Ensembl
Innerchr8:137687955..137876402hg19UCSC Ensembl
Innerchr8:137757137..137945584hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38188448
hg19188448
hg18188448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122346, nssv1122348, nssv1122352, nssv1122353, nssv1122355, nssv1122351, nssv1122350, nssv1122347, nssv1122345, nssv1122354, nssv1122349
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612408
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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