A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529036



Internal ID15109643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112890556..112893569hg38UCSC Ensembl
Innerchr9:115652836..115655849hg19UCSC Ensembl
Innerchr9:114692657..114695670hg18UCSC Ensembl
Innerchr9:112732391..112735404hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383014
hg193014
hg183014
hg173014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705747
Samples
Known GenesSLC46A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529036
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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