A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169814



Internal ID21478722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1361064..1361064hg38UCSC Ensembl
chrY:1429957..1429957hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608676
Supporting Variants
SamplesHG03486
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169814
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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