A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150589



Internal ID15876367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10054688..10100139hg38UCSC Ensembl
Innerchr18:10054685..10100136hg19UCSC Ensembl
Innerchr18:10044685..10090136hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3845452
hg1945452
hg1845452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576475
Supporting Variants
SamplesHGDP00830
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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