A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577113



Internal ID16364522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65324329..65370418hg38UCSC Ensembl
Innerchr18:62991565..63037654hg19UCSC Ensembl
Innerchr18:61142545..61188634hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3846090
hg1946090
hg1846090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv885017
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577113
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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