A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410706



Internal ID21068259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18828877..18860573hg38UCSC Ensembl
chr6:18829108..18860804hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3831697
hg1931697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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