A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610664



Internal ID21558969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1360994..1360994hg38UCSC Ensembl
chrY:1429887..1429887hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169813
SamplesHG03486
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610664
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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