A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526954



Internal ID15107561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14014568..14075301hg38UCSC Ensembl
Innerchr20:13995214..14055947hg19UCSC Ensembl
Innerchr20:13943214..14003947hg18UCSC Ensembl
Innerchr20:13943214..14003947hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3860734
hg1960734
hg1860734
hg1760734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703326
Samples
Known GenesMACROD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526954
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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