A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665219



Internal ID21613524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:268413..269347hg38UCSC Ensembl
chrY:135080..136014hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171194
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665219
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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