A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394907



Internal ID21052460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9561688..9573735hg38UCSC Ensembl
chr5:9561800..9573847hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3812048
hg1912048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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