A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526180



Internal ID15106787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95572438..95751280hg38UCSC Ensembl
Innerchr10:97332195..97511037hg19UCSC Ensembl
Innerchr10:97322185..97501027hg18UCSC Ensembl
Innerchr10:97322185..97501027hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38178843
hg19178843
hg18178843
hg17178843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702442
Samples
Known GenesALDH18A1, ENTPD1, TCTN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526180
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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