A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897653



Internal ID22672758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66189077..66191617hg38UCSC Ensembl
chr4:67054795..67057335hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382541
hg192541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897653
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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