A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944531



Internal ID22719997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72725459..72726158hg38UCSC Ensembl
chr13:73299597..73300296hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377334
Samples
Known GenesMZT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944531
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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