A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617994



Internal ID21566299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:323564..323564hg38UCSC Ensembl
chrY:234299..234299hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170673, nssv17170674
SamplesHG00512, HG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617994
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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