A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437335



Internal ID215926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151701373..151718019hg38UCSC Ensembl
chr3:151419161..151435807hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3816647
hg1916647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941194
Samples
Known GenesMIR548H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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