A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517495



Internal ID15444788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89407556..89459919hg38UCSC Ensembl
Innerchr9:92022471..92074834hg19UCSC Ensembl
Innerchr9:91212291..91264654hg18UCSC Ensembl
Innerchr9:89252025..89304388hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3852364
hg1952364
hg1852364
hg1752364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669291, nssv669587, nssv686773, nssv699273, nssv705978, nssv676888, nssv674112, nssv652189, nssv687647
Samples
Known GenesSEMA4D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517495
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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