A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011914



Internal ID19101132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161548149..161668399hg38UCSC Ensembl
Innerchr1:161517939..161638189hg19UCSC Ensembl
Innerchr1:159784563..159904813hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38120251
hg19120251
hg18120251
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv449n100
Supporting Variantsnssv3704785, nssv3704783, nssv3704784
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)nsv1011914
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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