A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522176



Internal ID15102783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37482145..37520456hg38UCSC Ensembl
Innerchr3:37523636..37561947hg19UCSC Ensembl
Innerchr3:37498640..37536951hg18UCSC Ensembl
Innerchr3:37498640..37536951hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3838312
hg1938312
hg1838312
hg1738312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694948
Samples
Known GenesITGA9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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