A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213036



Internal ID20780076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139271268..139288839hg38UCSC Ensembl
chr4:140192422..140209993hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3817572
hg1917572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390153
Supporting Variants
Samples
Known GenesMGARP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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