A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132095



Internal ID15985281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28049757..28051079hg38UCSC Ensembl
Innerchr9:28049755..28051077hg19UCSC Ensembl
Innerchr9:28039755..28041077hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381323
hg191323
hg181323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613958
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)nssv1132095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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