A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434609



Internal ID21092162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131121383..131498775hg38UCSC Ensembl
chr8:132133630..132511022hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38377393
hg19377393
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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