A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612559



Internal ID16399968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139750240..139793689hg38UCSC Ensembl
Innerchr8:140762483..140805932hg19UCSC Ensembl
Innerchr8:140831665..140875114hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3843450
hg1943450
hg1843450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12362n54
Supporting Variantsnssv1156883
Samples1780862156_A
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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