A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555486



Internal ID20928573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36768851..36769599hg38UCSC Ensembl
chr22:37164895..37165643hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074890
Samples
Known GenesIFT27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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