A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516776



Internal ID15097383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1215140..1253249hg38UCSC Ensembl
Innerchr20:1195784..1233893hg19UCSC Ensembl
Innerchr20:1143784..1181893hg18UCSC Ensembl
Innerchr20:1143784..1181893hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838110
hg1938110
hg1838110
hg1738110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678990, nssv670757
Samples
Known GenesRAD21L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516776
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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