A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456169



Internal ID234239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88006963..88007042hg38UCSC Ensembl
chr6:88716681..88716760hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456169
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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