A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139079



Internal ID338263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9801713..9813713hg38UCSC Ensembl
chrY:9639322..9651322hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3812001
hg1912001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738339
Samples
Known GenesTTTY22
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139079
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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