A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406004



Internal ID21063557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115026286..115031366hg38UCSC Ensembl
chr5:114361983..114367063hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg385081
hg195081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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