A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525532



Internal ID15106139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69224123..69228107hg38UCSC Ensembl
Innerchr9:71839039..71843023hg19UCSC Ensembl
Innerchr9:71028859..71032843hg18UCSC Ensembl
Innerchr9:69068593..69072577hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg383985
hg193985
hg183985
hg173985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701667
Samples
Known GenesTJP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525532
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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