A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413736



Internal ID21071289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96056706..96062398hg38UCSC Ensembl
chr6:96504582..96510274hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385693
hg195693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226305
Samples
Known GenesFUT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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