A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546014



Internal ID20919234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38685756..38691122hg38UCSC Ensembl
chr22:39081761..39087127hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073990
Samples
Known GenesJOSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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