A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547413



Internal ID20920614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30489552..30498296hg38UCSC Ensembl
chr22:30885539..30894283hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg388745
hg198745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073681
Samples
Known GenesSEC14L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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