A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418290



Internal ID21075843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126342101..126345200hg38UCSC Ensembl
chr8:127354346..127357445hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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