A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377069



Internal ID21034622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25926034..25930298hg38UCSC Ensembl
chr5:25926143..25930407hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg384265
hg194265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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