A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517522



Internal ID15444815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127162373..127213326hg38UCSC Ensembl
Innerchr9:129924652..129975605hg19UCSC Ensembl
Innerchr9:128964473..129015426hg18UCSC Ensembl
Innerchr9:127004206..127055159hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3850954
hg1950954
hg1850954
hg1750954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691532, nssv652268, nssv676706, nssv693652, nssv688354, nssv656905, nssv687646
Samples
Known GenesRALGPS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517522
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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