A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397289



Internal ID21054842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109658260..109658894hg38UCSC Ensembl
chr5:108993961..108994595hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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