A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014122



Internal ID19103342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161532055..161678435hg38UCSC Ensembl
Innerchr1:161501845..161648225hg19UCSC Ensembl
Innerchr1:159768469..159914849hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38146381
hg19146381
hg18146381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv451n100
Supporting Variantsnssv3497337
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)nsv1014122
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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