A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138921



Internal ID338105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:23139388..23145281hg38UCSC Ensembl
chrY:25285535..25291428hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg385894
hg195894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742977
Samples
Known GenesDAZ1, DAZ4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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