A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138966



Internal ID338150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120987835..120996835hg38UCSC Ensembl
chr1:149651203..149660201hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg389001
hg198999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16889981
Samples
Known GenesLINC00869
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138966
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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