A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442125



Internal ID220566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61326256..61384573hg38UCSC Ensembl
chr3:61311930..61370247hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3858318
hg1958318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442125
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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