A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672135



Internal ID21620440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1352880..1352981hg38UCSC Ensembl
chrY:1421773..1421874hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169807
SamplesHG00732
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672135
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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