A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434126



Internal ID21091679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:2485761..2918098hg38UCSC Ensembl
chr8:2342867..2775620hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38432338
hg19432754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434126
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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