A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756563



Internal ID20532423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6019033..6019033hg38UCSC Ensembl
chr10:6060996..6060996hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275519
Samples
Known GenesIL2RA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756563
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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