A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524034



Internal ID15451327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124808361..124811471hg38UCSC Ensembl
Innerchr9:127570640..127573750hg19UCSC Ensembl
Innerchr9:126610461..126613571hg18UCSC Ensembl
Innerchr9:124650194..124653304hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383111
hg193111
hg183111
hg173111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699897
Samples
Known GenesOLFML2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524034
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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