A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525090



Internal ID15452383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121811226..121819482hg38UCSC Ensembl
Innerchr9:124573505..124581761hg19UCSC Ensembl
Innerchr9:123613326..123621582hg18UCSC Ensembl
Innerchr9:121653059..121661315hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg388257
hg198257
hg188257
hg178257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701149
Samples
Known GenesMIR548AA1, MIR548D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525090
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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