A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033491



Internal ID18776024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170342284..170673434hg38UCSC Ensembl
Innerchr6:170651372..170982522hg19UCSC Ensembl
Innerchr6:170493297..170824447hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38331151
hg19331151
hg18331151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653094
Samples
Known GenesFAM120B, PDCD2, PSMB1, TBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033491
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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