A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145387



Internal ID15651887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133071778..133078923hg38UCSC Ensembl
Innerchr9:135947165..135954310hg19UCSC Ensembl
Innerchr9:134936986..134944131hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387146
hg197146
hg187146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615600
Supporting Variants
Samples
Known GenesCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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