A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953577



Internal ID22728856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58468613..58469539hg38UCSC Ensembl
chr20:57043669..57044595hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405297
Samples
Known GenesAPCDD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953577
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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