A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138423



Internal ID337607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22607281..22615388hg38UCSC Ensembl
chrY:24753428..24761535hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg388108
hg198108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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