A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576654



Internal ID16017377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37249923..37280895hg38UCSC Ensembl
Innerchr18:34829886..34860858hg19UCSC Ensembl
Innerchr18:33083884..33114856hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3830973
hg1930973
hg1830973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878964
Samples
Known GenesCELF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576654
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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