A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577905



Internal ID16018628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79731280..79765400hg38UCSC Ensembl
Innerchr18:77491280..77525400hg19UCSC Ensembl
Innerchr18:75592268..75626388hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3834121
hg1934121
hg1834121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6117n54
Supporting Variantsnssv890081
Samples
Known GenesCTDP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577905
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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