A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428049



Internal ID21085602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138778964..138796655hg38UCSC Ensembl
chr8:139791207..139808898hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3817692
hg1917692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166482
Samples
Known GenesCOL22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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