A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548595



Internal ID20921778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28501939..28515318hg38UCSC Ensembl
chr22:28897927..28911306hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3813380
hg1913380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073887
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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