A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525793



Internal ID15453086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233582905..233599722hg38UCSC Ensembl
Innerchr1:233718651..233735468hg19UCSC Ensembl
Innerchr1:231785274..231802091hg18UCSC Ensembl
Innerchr1:230025386..230042203hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3816818
hg1916818
hg1816818
hg1716818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv28n21
Supporting Variantsnssv701974
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525793
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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