A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902717



Internal ID22677878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153350090..153353787hg38UCSC Ensembl
chr5:152729650..152733347hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg383698
hg193698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902717
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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