A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577648



Internal ID16365057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73359044..73403724hg38UCSC Ensembl
Innerchr18:71026279..71070959hg19UCSC Ensembl
Innerchr18:69177259..69221939hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3844681
hg1944681
hg1844681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887374
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577648
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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