A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977882



Internal ID52647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181204612..181204663hg38UCSC Ensembl
chr5:180631612..180631663hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473790
Supporting Variants
Samples
Known GenesTRIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977882
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001873


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