A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316498



Internal ID20849578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218996275..219080663hg38UCSC Ensembl
chr1:219169617..219254005hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3884389
hg1984389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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