A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615440



Internal ID16402849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129434282..129454153hg38UCSC Ensembl
Innerchr9:132196561..132216432hg19UCSC Ensembl
Innerchr9:131236382..131256253hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3819872
hg1919872
hg1819872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12896n54
Supporting Variantsnssv1144790
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615440
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