A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618244



Internal ID21566549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1887490..1887490hg38UCSC Ensembl
chrY:1956383..1956383hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169484
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618244
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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