A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391494



Internal ID21049047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17341501..17357100hg38UCSC Ensembl
chr5:17341610..17357209hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3815600
hg1915600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5655n223
Supporting Variantsnssv18130242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391494
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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