A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666873



Internal ID21615180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2773534..2773645hg38UCSC Ensembl
chrY:2641575..2641686hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170640
SamplesHG00731
Known GenesXGPY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666873
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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