A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138922



Internal ID338106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145160587..145166587hg38UCSC Ensembl
chr1:149674796..149680733hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg386001
hg195938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890013
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138922
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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