A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577909



Internal ID16018632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79745247..79745871hg38UCSC Ensembl
Innerchr18:77505247..77505871hg19UCSC Ensembl
Innerchr18:75606235..75606859hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38625
hg19625
hg18625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv890089
Samples
Known GenesCTDP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577909
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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