A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404187



Internal ID21061740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81166801..81272000hg38UCSC Ensembl
chr6:81876518..81981717hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38105200
hg19105200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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