A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398857



Internal ID21056410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167414625..167454943hg38UCSC Ensembl
chr5:166841630..166881948hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3840319
hg1940319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129481
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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