A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554231



Internal ID20927337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42534201..42555300hg38UCSC Ensembl
chr22:42930207..42951306hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3821100
hg1921100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4723n223
Supporting Variantsnssv18207500
Samples
Known GenesSERHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554231
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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