A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401806



Internal ID21059359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15207455..15224994hg38UCSC Ensembl
chr6:15207686..15225225hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3817540
hg1917540
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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