A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538703



Internal ID20912017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37729521..37792224hg38UCSC Ensembl
chr22:38125528..38188231hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3862704
hg1962704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204637
Samples
Known GenesTRIOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538703
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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