A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457314



Internal ID235362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119061381..119067400hg38UCSC Ensembl
chr4:119982536..119988555hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg386020
hg196020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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