A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624296



Internal ID21572601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1888318..1888318hg38UCSC Ensembl
chrY:1957211..1957211hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169488
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624296
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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