A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402467



Internal ID22460337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39150658..39151389hg38UCSC Ensembl
chr22:39546663..39547394hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977407
Supporting Variants
Samples
Known GenesCBX7
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402467
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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