A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128524



Internal ID15981710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10661370..10688795hg38UCSC Ensembl
Innerchr9:10661370..10688795hg19UCSC Ensembl
Innerchr9:10651370..10678795hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3827426
hg1927426
hg1827426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613400
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)nssv1128524
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