A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544156



Internal ID20917395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37772607..37786629hg38UCSC Ensembl
chr22:38168614..38182636hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3814023
hg1914023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204639
Samples
Known GenesTRIOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544156
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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