A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138357



Internal ID337541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145168587..145248587hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3880001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138357
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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