A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615218



Internal ID16402627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113602846..113628789hg38UCSC Ensembl
Innerchr9:116365126..116391069hg19UCSC Ensembl
Innerchr9:115404947..115430890hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3825944
hg1925944
hg1825944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141259
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615218
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