A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907362



Internal ID22682570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19005823..19079146hg38UCSC Ensembl
chr5:19005932..19079255hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3873324
hg1973324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907362
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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