A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384708



Internal ID21042261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:44708145..44717230hg38UCSC Ensembl
chr5:44708247..44717332hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg389086
hg199086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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