A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954139



Internal ID22729399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50632086..50632809hg38UCSC Ensembl
chr20:49248623..49249346hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398995
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954139
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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