A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138813



Internal ID337997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144966587..146310000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381343414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16889803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138813
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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