A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071205



Internal ID21411304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6031444..6031493hg38UCSC Ensembl
chr10:6073407..6073456hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601114
Supporting Variants
SamplesHG00513
Known GenesIL2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071205
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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