A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522175



Internal ID15449468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182372131..182441639hg38UCSC Ensembl
Innerchr3:182089919..182159427hg19UCSC Ensembl
Innerchr3:183572613..183642121hg18UCSC Ensembl
Innerchr3:183572621..183642129hg17UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3869509
hg1969509
hg1869509
hg1769509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv306n21
Supporting Variantsnssv694947
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522175
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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