A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919682



Internal ID22694904
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 Variantsnssv17362781
Samples
Known GenesIL2RA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919682
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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