A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056236



Internal ID21965469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44252443..44252548hg38UCSC Ensembl
chr22:44648323..44648428hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646125
Samples
Known GenesKIAA1644
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056236
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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