A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548067



Internal ID15988790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161587939..161654964hg38UCSC Ensembl
Innerchr1:161557729..161624754hg19UCSC Ensembl
Innerchr1:159824353..159891378hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3867026
hg1967026
hg1867026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv607n54
Supporting Variantsnssv727691, nssv727690
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548067
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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