A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457011



Internal ID235067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53938061..53938131hg38UCSC Ensembl
chr6:53802859..53802929hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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