A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398869



Internal ID21056422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168128170..168135242hg38UCSC Ensembl
chr5:167555175..167562247hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg387073
hg197073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129522
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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