A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015116



Internal ID19104333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623061..161667408hg38UCSC Ensembl
Innerchr1:161592851..161637198hg19UCSC Ensembl
Innerchr1:159859475..159903822hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3844348
hg1944348
hg1844348
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv452n100
Supporting Variantsnssv3498320, nssv3497052, nssv3484785, nssv3704792
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)nsv1015116
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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