A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528431



Internal ID15109038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56248749..56264206hg38UCSC Ensembl
Innerchr20:54823805..54839262hg19UCSC Ensembl
Innerchr20:54257212..54272669hg18UCSC Ensembl
Innerchr20:54257212..54272669hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3815458
hg1915458
hg1815458
hg1715458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705024
Samples
Known GenesMC3R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528431
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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