A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026980



Internal ID18769512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160438325..160798037hg38UCSC Ensembl
Innerchr5:159865332..160225044hg19UCSC Ensembl
Innerchr5:159797910..160157622hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38359713
hg19359713
hg18359713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648227
Samples
Known GenesATP10B, MIR146A, MIR3142
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026980
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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