A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403720



Internal ID21061273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11869377..11899188hg38UCSC Ensembl
chr6:11869610..11899421hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3829812
hg1929812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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