A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548074



Internal ID15988797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623299..161671187hg38UCSC Ensembl
Innerchr1:161593089..161640977hg19UCSC Ensembl
Innerchr1:159859713..159907601hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3847889
hg1947889
hg1847889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv727700
Samples
Known GenesFCGR2B, FCGR3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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