A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615518



Internal ID16402927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130269048..130272066hg38UCSC Ensembl
Innerchr9:133031327..133034345hg19UCSC Ensembl
Innerchr9:132071148..132074166hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383019
hg193019
hg183019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12909n54
Supporting Variantsnssv1145185, nssv1145186
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615518
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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