A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444330



Internal ID222706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68975462..68975517hg38UCSC Ensembl
chr3:69024613..69024668hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934040
Samples
Known GenesEOGT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444330
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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