A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970582



Internal ID47714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91616506..91619188hg38UCSC Ensembl
chr5:90912323..90915005hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382683
hg192683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970582
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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