A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704776



Internal ID19003057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161543969..161668399hg38UCSC Ensembl
Innerchr1:161513759..161638189hg19UCSC Ensembl
Innerchr1:159780383..159904813hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38124431
hg19124431
hg18124431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998753
Supporting Variants
Samples
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3704776
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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