A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459213



Internal ID237229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55690000..55741500hg38UCSC Ensembl
chr6:55554798..55606298hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3851501
hg1951501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459213
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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