A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426733



Internal ID21084286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36391001..36410600hg38UCSC Ensembl
chr8:36248519..36268118hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3819600
hg1919600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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