A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611803



Internal ID16052526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97029431..97250016hg38UCSC Ensembl
Innerchr8:98041659..98262244hg19UCSC Ensembl
Innerchr8:98110835..98331420hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38220586
hg19220586
hg18220586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118153
Samples
Known GenesCPQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611803
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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