A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887828



Internal ID22662825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174958477..174958561hg38UCSC Ensembl
chr5:174385480..174385564hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413288
Samples
Known GenesFLJ16171
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887828
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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