A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012357



Internal ID19101575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161648889hg38UCSC Ensembl
Innerchr1:161496900..161618679hg19UCSC Ensembl
Innerchr1:159763524..159885303hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38121780
hg19121780
hg18121780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n100
Supporting Variantsnssv3495565
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)nsv1012357
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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