A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449729



Internal ID227957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32495730..32500829hg38UCSC Ensembl
chr3:32537222..32542321hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932345
Samples
Known GenesCMTM6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449729
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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