A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669646



Internal ID21617951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5115736..5116050hg38UCSC Ensembl
chrY:4983777..4984091hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170585
SamplesNA18534
Known GenesPCDH11Y
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669646
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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