A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980966



Internal ID54685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11402335..11402470hg38UCSC Ensembl
chr6:11402568..11402703hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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