A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427092



Internal ID21084645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126443822..126456944hg38UCSC Ensembl
chr8:127456067..127469189hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3813123
hg1913123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427092
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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