A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331613



Internal ID20864777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2746401..2792300hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3845900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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