A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv727696



Internal ID15674966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161599629..161654964hg38UCSC Ensembl
Innerchr1:161569419..161624754hg19UCSC Ensembl
Innerchr1:159836043..159891378hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3855336
hg1955336
hg1855336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548070
Supporting Variants
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)nssv727696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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