A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904189



Internal ID22679365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2305973..2307101hg38UCSC Ensembl
chr5:2306087..2307215hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381129
hg191129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425948
Samples
Known GenesLOC100506858
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904189
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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