A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611835



Internal ID16399244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:104078752..104141558hg38UCSC Ensembl
Innerchr8:105090980..105153786hg19UCSC Ensembl
Innerchr8:105160156..105222962hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3862807
hg1962807
hg1862807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118228
Samples
Known GenesRIMS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611835
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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