A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394218



Internal ID21051771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:90764607..90865321hg38UCSC Ensembl
chr4:91685758..91786472hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38100715
hg19100715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215272
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394218
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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