A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407770



Internal ID21065323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158217323..158228242hg38UCSC Ensembl
chr5:157644331..157655250hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3810920
hg1910920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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