A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520089



Internal ID15447382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:200331171..200360430hg38UCSC Ensembl
Innerchr1:200300299..200329558hg19UCSC Ensembl
Innerchr1:198566922..198596181hg18UCSC Ensembl
Innerchr1:197031956..197061215hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3829260
hg1929260
hg1829260
hg1729260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv23n21
Supporting Variantsnssv697218
Samples
Known GenesLINC00862
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520089
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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