A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412874



Internal ID21070427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84477618..84487935hg38UCSC Ensembl
chr5:83773436..83783753hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3810318
hg1910318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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