A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577819



Internal ID16018542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78980085..78980923hg38UCSC Ensembl
Innerchr18:76740085..76740923hg19UCSC Ensembl
Innerchr18:74841073..74841911hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38839
hg19839
hg18839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6103n54
Supporting Variantsnssv888903
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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