A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531165



Internal ID307129
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 StatusM
Merged Variants
Supporting Variantsnssv17732127
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531165
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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