A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610189



Internal ID16050912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8732927..8807430hg38UCSC Ensembl
Innerchr8:8590437..8664940hg19UCSC Ensembl
Innerchr8:8627847..8702350hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3874504
hg1974504
hg1874504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105956
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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