A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132098



Internal ID15985284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28049798..28050779hg38UCSC Ensembl
Innerchr9:28049796..28050777hg19UCSC Ensembl
Innerchr9:28039796..28040777hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38982
hg19982
hg18982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613960
Supporting Variants
Samples
Known GenesLINGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1132098
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