A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387542



Internal ID22445412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96506147..96507024hg38UCSC Ensembl
chr14:96972484..96973361hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968807
Supporting Variants
Samples
Known GenesPAPOLA
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387542
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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