A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525274



Internal ID15452567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104778620..104822678hg38UCSC Ensembl
Innerchr1:105321242..105365300hg19UCSC Ensembl
Innerchr1:105122765..105166823hg18UCSC Ensembl
Innerchr1:105033263..105077321hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3844059
hg1944059
hg1844059
hg1744059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701375
Samples
Known GenesMIR548H3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525274
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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