A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044442



Internal ID21953724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29153085..29155172hg38UCSC Ensembl
chr22:29549073..29551160hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646271
Samples
Known GenesKREMEN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044442
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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