A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380971



Internal ID21038524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99555101..99559200hg38UCSC Ensembl
chr4:100476258..100480357hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121333
Samples
Known GenesTRMT10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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