A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552122



Internal ID20925252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29061492..29065044hg38UCSC Ensembl
chr22:29457480..29461032hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg383553
hg193553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072996
Samples
Known GenesC22orf31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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