A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449767



Internal ID227995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186668731..186706833hg38UCSC Ensembl
chr3:186386520..186424622hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3838103
hg1938103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943376
Samples
Known GenesHRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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