A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978446



Internal ID53008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2791334..2809985hg38UCSC Ensembl
chr6:2791568..2810219hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3818652
hg1918652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978446
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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