A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525407



Internal ID8419682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:993026..993795hg38UCSC Ensembl
Innerchr20:973669..974438hg19UCSC Ensembl
Innerchr20:921669..922438hg18UCSC Ensembl
Innerchr20:921669..922438hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38770
hg19770
hg18770
hg17770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701531
Samples
Known GenesRSPO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525407
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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