A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526715



Internal ID15454008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19145437..19209548hg38UCSC Ensembl
Innerchr9:19145435..19209546hg19UCSC Ensembl
Innerchr9:19135435..19199546hg18UCSC Ensembl
Innerchr9:19135435..19199546hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3864112
hg1964112
hg1864112
hg1764112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703055
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526715
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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