A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577796



Internal ID16365205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78978993..78980500hg38UCSC Ensembl
Innerchr18:76738993..76740500hg19UCSC Ensembl
Innerchr18:74839981..74841488hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381508
hg191508
hg181508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv888833
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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