A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491802



Internal ID19079443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161623061..161649256hg38UCSC Ensembl
Innerchr1:161592851..161619046hg19UCSC Ensembl
Innerchr1:159859475..159885670hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3826196
hg1926196
hg1826196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009190
Supporting Variants
Samples
Known GenesFCGR3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3491802
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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