A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577050



Internal ID16017773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:58664431..58732147hg38UCSC Ensembl
Innerchr18:56331663..56399379hg19UCSC Ensembl
Innerchr18:54482643..54550359hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3867717
hg1967717
hg1867717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884909
Samples
Known GenesMALT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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