A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437506



Internal ID216091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33160613..33160665hg38UCSC Ensembl
chr3:33202105..33202157hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932418
Samples
Known GenesSUSD5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437506
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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