A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525959



Internal ID15106566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:184614160..184625886hg38UCSC Ensembl
Innerchr1:184583294..184595020hg19UCSC Ensembl
Innerchr1:182849917..182861643hg18UCSC Ensembl
Innerchr1:181314951..181326677hg17UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3811727
hg1911727
hg1811727
hg1711727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv20n21
Supporting Variantsnssv702170
Samples
Known GenesC1orf21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525959
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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