A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390001



Internal ID21047554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:80094338..80095043hg38UCSC Ensembl
chr4:81015492..81016197hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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