A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213765



Internal ID20780805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163760863..163806646hg38UCSC Ensembl
chr4:164682015..164727798hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3845784
hg1945784
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390578
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213765
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00025


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