A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496987



Internal ID19084628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161647212hg38UCSC Ensembl
Innerchr1:161496900..161617002hg19UCSC Ensembl
Innerchr1:159763524..159883626hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38120103
hg19120103
hg18120103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013229
Supporting Variants
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)nssv3496987
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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