A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410566



Internal ID21068119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91518351..91537843hg38UCSC Ensembl
chr6:92228069..92247561hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3819493
hg1919493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228170
Samples
Known GenesMIR4643
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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