A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577797



Internal ID16365206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78978993..78980611hg38UCSC Ensembl
Innerchr18:76738993..76740611hg19UCSC Ensembl
Innerchr18:74839981..74841599hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381619
hg191619
hg181619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6099n54
Supporting Variantsnssv888834
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577797
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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