A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112441



Internal ID22021674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45315675..45315675hg38UCSC Ensembl
chr22:45711556..45711556hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640427
Samples
Known GenesFAM118A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112441
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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