A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144546



Internal ID343751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31961764..32011528hg38UCSC Ensembl
chr18:29541727..29591491hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3849765
hg1949765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717110
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144546
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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