A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328590



Internal ID20861738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155574675..155583937hg38UCSC Ensembl
chr1:155544466..155553728hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg389263
hg199263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200528
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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