A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619057



Internal ID20992128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111461401..111462800hg38UCSC Ensembl
chr6:111782604..111784003hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135409
Samples
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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