A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526701



Internal ID15453994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53154152..53163788hg38UCSC Ensembl
Innerchr20:51770691..51780327hg19UCSC Ensembl
Innerchr20:51204098..51213734hg18UCSC Ensembl
Innerchr20:51204098..51213734hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389637
hg199637
hg189637
hg179637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703040
Samples
Known GenesTSHZ2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526701
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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