A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732520



Internal ID20508444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6031447..6031499hg38UCSC Ensembl
chr10:6073410..6073462hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267053
Samples
Known GenesIL2RA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732520
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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