A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435708



Internal ID21093261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5965928..5967383hg38UCSC Ensembl
chr10:6007891..6009346hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982250
Samples
Known GenesIL15RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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