A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444896



Internal ID223260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154872810..154875110hg38UCSC Ensembl
chr3:154590599..154592899hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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