A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582132



Internal ID20955203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51059668..51060548hg38UCSC Ensembl
chr14:51526386..51527266hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229756
Samples
Known GenesTRIM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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