A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367336



Internal ID21024889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164764001..164803800hg38UCSC Ensembl
chr3:164481789..164521588hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3839800
hg1939800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367336
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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