A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997933



Internal ID19157469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623061..161667183hg38UCSC Ensembl
Innerchr1:161592851..161636973hg19UCSC Ensembl
Innerchr1:159859475..159903597hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3844123
hg1944123
hg1844123
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv452n100
Supporting Variantsnssv3487026, nssv3704791
Samples
Known GenesFCGR2B, FCGR3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997933
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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