A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000695



Internal ID19089912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161649018hg38UCSC Ensembl
Innerchr1:161496900..161618808hg19UCSC Ensembl
Innerchr1:159763524..159885432hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38121909
hg19121909
hg18121909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n100
Supporting Variantsnssv3500783
Samples
Known GenesFCGR2C, 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)nsv1000695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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