A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424995



Internal ID203969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15194679..15196803hg38UCSC Ensembl
chrY:17306559..17308683hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg382125
hg192125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424995
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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