A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381592



Internal ID21039145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35869091..35869628hg38UCSC Ensembl
chr5:35869193..35869730hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213413
Samples
Known GenesIL7R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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