A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732127



Internal ID155793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34817117..34817212hg38UCSC Ensembl
chr20:33404920..33405015hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531165
Supporting Variants
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732127
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.256285


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