A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458441



Internal ID236462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7093269..7115543hg38UCSC Ensembl
chr5:7093382..7115656hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3822275
hg1922275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458441
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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