A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898417



Internal ID22673531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2070061..2070282hg38UCSC Ensembl
chr4:2071788..2072009hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898417
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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