A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524920



Internal ID15452213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24659280..24702918hg38UCSC Ensembl
Innerchr20:24639916..24683554hg19UCSC Ensembl
Innerchr20:24587916..24631554hg18UCSC Ensembl
Innerchr20:24587916..24631554hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3843639
hg1943639
hg1843639
hg1743639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700932
Samples
Known GenesSYNDIG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524920
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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