A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169810



Internal ID21447633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1360220..1360305hg38UCSC Ensembl
chrY:1429113..1429198hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672372
Supporting Variants
SamplesHG00732
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169810
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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