A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577078



Internal ID16364487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62039466..62043844hg38UCSC Ensembl
Innerchr18:59706699..59711077hg19UCSC Ensembl
Innerchr18:57857679..57862057hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384379
hg194379
hg184379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5964n54
Supporting Variantsnssv884947
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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