A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013029



Internal ID19102247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161532055..161649018hg38UCSC Ensembl
Innerchr1:161501845..161618808hg19UCSC Ensembl
Innerchr1:159768469..159885432hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38116964
hg19116964
hg18116964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n100
Supporting Variantsnssv3704771
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)nsv1013029
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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