A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667750



Internal ID21616055
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 StatusM
Merged Variants
Supporting Variantsnssv17169809
SamplesHG03486
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667750
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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