A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv888907



Internal ID15836177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78980085..78994367hg38UCSC Ensembl
Innerchr18:76740085..76754367hg19UCSC Ensembl
Innerchr18:74841073..74855355hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3814283
hg1914283
hg1814283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577821
Supporting Variants
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv888907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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