A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517609



Internal ID15444902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104587359..104602301hg38UCSC Ensembl
Innerchr9:107349640..107364582hg19UCSC Ensembl
Innerchr9:106389461..106404403hg18UCSC Ensembl
Innerchr9:104429195..104444137hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3814943
hg1914943
hg1814943
hg1714943
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699019, nssv682077, nssv675656, nssv652498, nssv698453, nssv678114, nssv693000, nssv675893, nssv693082, nssv675743, nssv652679, nssv679290, nssv685718, nssv663914, nssv664075, nssv689781, nssv658217, nssv656424, nssv667016, nssv668827, nssv672821, nssv663996, nssv670503, nssv689228, nssv666808, nssv653399, nssv673743, nssv661890, nssv667763, nssv684586, nssv658779, nssv691433, nssv679458, nssv687339, nssv680477, nssv661733, nssv678656, nssv684726, nssv689300
Samples
Known GenesOR13C5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517609
Frequency
Sample Size2026
Observed Gain1
Observed Loss38
Observed Complex0
Frequencyn/a


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