A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537808



Internal ID20911140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37933415..37948986hg38UCSC Ensembl
chr22:38329422..38344993hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3815572
hg1915572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204641
Samples
Known GenesC22orf23, MICALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537808
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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