A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615997



Internal ID16056720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136977199..136984376hg38UCSC Ensembl
Innerchr9:139871651..139878828hg19UCSC Ensembl
Innerchr9:138991472..138998649hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387178
hg197178
hg187178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148349
Samples
Known GenesLCNL1, PTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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