A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132128



Internal ID15985314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28544377..28711489hg38UCSC Ensembl
Innerchr9:28544375..28711487hg19UCSC Ensembl
Innerchr9:28534375..28701487hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38167113
hg19167113
hg18167113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613985
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)nssv1132128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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