A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551607



Internal ID20924740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20890627..20896623hg38UCSC Ensembl
chr22:21244915..21250911hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg385997
hg195997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072972
Samples
Known GenesSNAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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