A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456365



Internal ID234435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160490775..160496297hg38UCSC Ensembl
chr6:160911807..160917329hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385523
hg195523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990839
Samples
Known GenesLPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456365
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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