A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522145



Internal ID15449438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121918088..121941053hg38UCSC Ensembl
Innerchr9:124680367..124703332hg19UCSC Ensembl
Innerchr9:123720188..123743153hg18UCSC Ensembl
Innerchr9:121759921..121782886hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3822966
hg1922966
hg1822966
hg1722966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694918
Samples
Known GenesMIR548AA1, MIR548D1, TTLL11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522145
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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