A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391698



Internal ID21049251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45080575..45081088hg38UCSC Ensembl
chr4:45082592..45083105hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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