A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431484



Internal ID21089037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57458647..57481984hg38UCSC Ensembl
chr8:58371206..58394543hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3823338
hg1923338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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