A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664599



Internal ID21612904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18828015..18828316hg38UCSC Ensembl
chrY:20989901..20990202hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169481
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664599
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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