A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432020



Internal ID21089573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133111767..133122905hg38UCSC Ensembl
chr8:134124011..134135149hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3811139
hg1911139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219883
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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