A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128784



Internal ID15981970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14590807..14616592hg38UCSC Ensembl
Innerchr9:14590805..14616590hg19UCSC Ensembl
Innerchr9:14580805..14606590hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3825786
hg1925786
hg1825786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613640
Supporting Variants
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128784
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