A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401290



Internal ID21058843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91983689..92144408hg38UCSC Ensembl
chr6:92693407..92854126hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38160720
hg19160720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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