A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009190



Internal ID19098408
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483318, nssv3497912, nssv3491802, nssv3501254
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)nsv1009190
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer