A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576566



Internal ID16363975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22023052..22066442hg38UCSC Ensembl
Innerchr18:19603013..19646403hg19UCSC Ensembl
Innerchr18:17857011..17900401hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3843391
hg1943391
hg1843391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878492
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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