A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394912



Internal ID21052465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94164801..94166000hg38UCSC Ensembl
chr4:95085952..95087151hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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