A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128565



Internal ID15981751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11651144..11935261hg38UCSC Ensembl
Innerchr9:11651144..11935261hg19UCSC Ensembl
Innerchr9:11641144..11925261hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38284118
hg19284118
hg18284118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613442
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128565
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