A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437567



Internal ID216152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134647586..134651284hg38UCSC Ensembl
chr3:134366428..134370126hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383699
hg193699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939267
Samples
Known GenesKY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437567
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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