A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414651



Internal ID21072204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81414416..81414780hg38UCSC Ensembl
chr5:80710235..80710599hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134153
Samples
Known GenesRNU5D-1, RNU5E-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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