A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138532



Internal ID337716
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 StatusM
Merged Variants
Supporting Variantsnssv17742806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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