A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426367



Internal ID21083920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58544501..58556600hg38UCSC Ensembl
chr8:59457060..59469159hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233488
Samples
Known GenesSDCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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