A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv727692



Internal ID15674962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161587939..161671187hg38UCSC Ensembl
Innerchr1:161557729..161640977hg19UCSC Ensembl
Innerchr1:159824353..159907601hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3883249
hg1983249
hg1883249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548068
Supporting Variants
Samples
Known GenesFCGR2B, FCGR2C, FCGR3B, HSPA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv727692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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