A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169809



Internal ID21478726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1353297..1353923hg38UCSC Ensembl
chrY:1422190..1422816hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667750
Supporting Variants
SamplesHG03486
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169809
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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