A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437088



Internal ID21094641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22625767..22648931hg38UCSC Ensembl
chr11:22647313..22670477hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3823165
hg1923165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188507
Samples
Known GenesFANCF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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