A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610776



Internal ID16051499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23087182..23183569hg38UCSC Ensembl
Innerchr8:22944695..23041082hg19UCSC Ensembl
Innerchr8:23000640..23097027hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3896388
hg1996388
hg1896388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12057n54
Supporting Variantsnssv1107480
Samples
Known GenesLOC254896, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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