A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543639



Internal ID20916885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42536101..42555200hg38UCSC Ensembl
chr22:42932107..42951206hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3819100
hg1919100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4723n223
Supporting Variantsnssv18207502
Samples
Known GenesSERHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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