A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423725



Internal ID21081278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9491977..9496515hg38UCSC Ensembl
chr8:9349487..9354025hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg384539
hg194539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423725
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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