A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980678



Internal ID54498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15761720..15774651hg38UCSC Ensembl
chr6:15761951..15774882hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3812932
hg1912932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980678
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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