A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137902



Internal ID337083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20107300..20191528hg38UCSC Ensembl
chrY:22269186..22353414hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3884229
hg1984229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742862
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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