A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv879928



Internal ID16173884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40640135..40685484hg38UCSC Ensembl
Innerchr18:38220099..38265448hg19UCSC Ensembl
Innerchr18:36474097..36519446hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3845350
hg1945350
hg1845350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576673
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv879928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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