A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439063



Internal ID217609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8765222..8768819hg38UCSC Ensembl
chr4:8766948..8770545hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg383598
hg193598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439063
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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