A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611646



Internal ID16052369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84136455..84200142hg38UCSC Ensembl
Innerchr8:85048690..85112377hg19UCSC Ensembl
Innerchr8:85211245..85274932hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3863688
hg1963688
hg1863688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1117337
Samples
Known GenesRALYL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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