A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684108



Internal ID21205963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6031443..6031508hg38UCSC Ensembl
chr10:6073406..6073471hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789245
Supporting Variants
Samples
Known GenesIL2RA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684108
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.265625


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