A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621566



Internal ID21569871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12485499..12485499hg38UCSC Ensembl
chrY:14597299..14597299hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169605
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621566
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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