A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449663



Internal ID227894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78821949..78822922hg38UCSC Ensembl
chr3:78871099..78872072hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38974
hg19974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934361
Samples
Known GenesROBO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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