A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669653



Internal ID21617958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:5107772..5108097hg38UCSC Ensembl
chrY:4975813..4976138hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170584
SamplesNA18534
Known GenesPCDH11Y
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669653
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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