A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426707



Internal ID205631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15883288..15896488hg38UCSC Ensembl
chrY:17995168..18008368hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3813201
hg1913201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426707
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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