A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597460



Internal ID21546074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6022805..6022877hg38UCSC Ensembl
chr10:6064768..6064840hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071200
SamplesHG00731
Known GenesIL2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597460
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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