A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610153



Internal ID16050876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8240557..8597021hg38UCSC Ensembl
Innerchr8:8098079..8454531hg19UCSC Ensembl
Innerchr8:8135489..8491941hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38356465
hg19356453
hg18356453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105886
Samples
Known GenesFAM86B3P, SGK223
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610153
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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