A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576244



Internal ID16016967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:609954..620709hg38UCSC Ensembl
Innerchr18:609954..620709hg19UCSC Ensembl
Innerchr18:599954..610709hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3810756
hg1910756
hg1810756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877296
Samples
Known GenesCLUL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576244
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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