A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957157



Internal ID22732297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45988255..45998280hg38UCSC Ensembl
chr20:44616894..44626919hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3810026
hg1910026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957157
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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