A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071202



Internal ID21980435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55897000..55897000hg38UCSC Ensembl
chr5:55192828..55192828hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550580
Samples
Known GenesIL31RA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071202
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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