A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902101



Internal ID22677255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87005383..87010429hg38UCSC Ensembl
chr5:86301200..86306246hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385047
hg195047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902101
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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