A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618383



Internal ID21566688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2773534..2773534hg38UCSC Ensembl
chrY:2641575..2641575hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170641
SamplesHG03371
Known GenesXGPY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618383
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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