A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615574



Internal ID16402983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132733601..132751450hg38UCSC Ensembl
Innerchr9:135608988..135626837hg19UCSC Ensembl
Innerchr9:134598809..134616658hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3817850
hg1917850
hg1817850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145328
Samples
Known GenesAK8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615574
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