A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576281



Internal ID16363690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1901533..1980667hg38UCSC Ensembl
Innerchr18:1901534..1980668hg19UCSC Ensembl
Innerchr18:1891534..1970668hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3879135
hg1979135
hg1879135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5816n54
Supporting Variantsnssv877340, nssv877341, nssv877342
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576281
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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