A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137884



Internal ID337065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11679173..11687060hg38UCSC Ensembl
chrY:13799879..13807766hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg387888
hg197888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137884
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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