A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899880



Internal ID22675016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152852172..152852632hg38UCSC Ensembl
chr5:152231732..152232192hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899880
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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