A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982337



Internal ID55573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25893695..25905345hg38UCSC Ensembl
chr6:25893923..25905573hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3811651
hg1911651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982337
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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