A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407909



Internal ID21065462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11044901..11050200hg38UCSC Ensembl
chr6:11045134..11050433hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216805
Samples
Known GenesELOVL2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407909
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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