A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596482



Internal ID21514005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:33420..33420hg38UCSC Ensembl
chrY:33420..33420hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170535
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596482
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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