A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375020



Internal ID21032573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18179361..18184302hg38UCSC Ensembl
chr4:18180984..18185925hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg384942
hg194942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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