A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140462



Internal ID339655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102632549..102632621hg38UCSC Ensembl
chr5:101968253..101968325hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971724
Samples
Known GenesLINC00491
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140462
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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