A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960629



Internal ID22735601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24517514..25490454hg38UCSC Ensembl
chr20:24498150..25471090hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38972941
hg19972941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407677
Samples
Known GenesABHD12, ACSS1, APMAP, CST7, ENTPD6, GINS1, LOC284798, NINL, PYGB, SYNDIG1, VSX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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