A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405593



Internal ID21063146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114074929..114081398hg38UCSC Ensembl
chr5:113410626..113417095hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg386470
hg196470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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