A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518602



Internal ID15099209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127870863..127898531hg38UCSC Ensembl
Innerchr9:130633142..130660810hg19UCSC Ensembl
Innerchr9:129672963..129700631hg18UCSC Ensembl
Innerchr9:127712696..127740364hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3827669
hg1927669
hg1827669
hg1727669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv497n21
Supporting Variantsnssv696048
Samples
Known GenesAK1, ST6GALNAC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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