A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400563



Internal ID21058116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89252401..89253600hg38UCSC Ensembl
chr5:88548218..88549417hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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