A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669921



Internal ID21618226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18169597..18169917hg38UCSC Ensembl
chrY:20331483..20331803hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169865
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669921
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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