A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169811



Internal ID21482421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1360820..1360820hg38UCSC Ensembl
chrY:1429713..1429713hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618300
Supporting Variants
SamplesHG03732
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169811
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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