A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010408



Internal ID21919751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137083422..137169565hg38UCSC Ensembl
chr6:137404559..137490702hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3886144
hg1986144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567062
Samples
Known GenesIL22RA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010408
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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