A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526190



Internal ID15106797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108335844..108406767hg38UCSC Ensembl
Innerchr3:108054691..108125614hg19UCSC Ensembl
Innerchr3:109537381..109608304hg18UCSC Ensembl
Innerchr3:109537381..109608304hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3870924
hg1970924
hg1870924
hg1770924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702452
Samples
Known GenesHHLA2, MYH15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526190
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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