A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618578



Internal ID21566883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6466313..6466313hg38UCSC Ensembl
chrY:6334354..6334354hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171018
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618578
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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