A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890249



Internal ID22665275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167302742..167303556hg38UCSC Ensembl
chr5:166729747..166730561hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414963
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890249
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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