A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435026



Internal ID213684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151685749..151701587hg38UCSC Ensembl
chr3:151403537..151419375hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3815839
hg1915839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941192
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435026
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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