A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055236



Internal ID21964469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29159391..29166817hg38UCSC Ensembl
chr22:29555379..29562805hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg387427
hg197427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638798
Samples
Known GenesKREMEN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055236
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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