A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459788



Internal ID237797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37336817..37348588hg38UCSC Ensembl
chr6:37304593..37316364hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3811772
hg1911772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459788
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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