A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005156



Internal ID19094373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161527110..161648449hg38UCSC Ensembl
Innerchr1:161496900..161618239hg19UCSC Ensembl
Innerchr1:159763524..159884863hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38121340
hg19121340
hg18121340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv448n100
Supporting Variantsnssv3704750, nssv3704751
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)nsv1005156
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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