A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414204



Internal ID21071757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:101833955..102167219hg38UCSC Ensembl
chr5:101169659..101502923hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38333265
hg19333265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5848n223
Supporting Variantsnssv18121394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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