A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14432824



Internal ID22175712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26242619..26242673hg38UCSC Ensembl
chr22:26638585..26638639hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202122
Supporting Variants
SamplesHG00514
Known GenesSEZ6L
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14432824
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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