A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370224



Internal ID22259598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60605282..60612178hg38UCSC Ensembl
chr14:61072000..61078896hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg386897
hg196897
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3247784
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370224
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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