A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895292



Internal ID22670372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67041726..67042272hg38UCSC Ensembl
chr5:66337554..66338100hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422853
Samples
Known GenesMAST4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895292
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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