A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425907



Internal ID204858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32176556..32177600hg38UCSC Ensembl
chr20:30764359..30765403hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425907
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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