A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443228



Internal ID221629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77214367..77216621hg38UCSC Ensembl
chr3:77263518..77265772hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg382255
hg192255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16935462
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443228
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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