A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896869



Internal ID22671965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145225740..145225962hg38UCSC Ensembl
chr5:144605303..144605525hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896869
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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