A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008903



Internal ID18751434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161550780..161668399hg38UCSC Ensembl
Innerchr1:161520570..161638189hg19UCSC Ensembl
Innerchr1:159787194..159904813hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38117620
hg19117620
hg18117620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv450n100
Supporting Variantsnssv3704788
Samples
Known GenesFCGR2B, FCGR2C, 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)nsv1008903
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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