A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868592



Internal ID22643470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43631359..43644373hg38UCSC Ensembl
chr22:44027239..44040253hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3813015
hg1913015
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483654, nssv17483655
Samples
Known GenesEFCAB6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868592
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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