A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451660



Internal ID229836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157563867..157563927hg38UCSC Ensembl
chr3:157281656..157281716hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940099
Samples
Known GenesC3orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451660
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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