A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554663



Internal ID20927757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28031005..28042422hg38UCSC Ensembl
chr22:28426993..28438410hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3811418
hg1911418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073235
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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