A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742806



Internal ID166472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15563927..15566738hg38UCSC Ensembl
chrY:17675807..17678618hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg382812
hg192812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742806
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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