A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391916



Internal ID21049469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99562564..99562860hg38UCSC Ensembl
chr4:100483721..100484017hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214417
Samples
Known GenesTRMT10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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