A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444457



Internal ID222827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36526601..36528366hg38UCSC Ensembl
chr3:36568093..36569858hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932563
Samples
Known GenesSTAC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444457
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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