A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389256



Internal ID21046809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4894349..4903722hg38UCSC Ensembl
chr5:4894462..4903835hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg389374
hg199374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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