A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386314



Internal ID21043867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25467079..25719660hg38UCSC Ensembl
chr5:25467188..25719769hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38252582
hg19252582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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