A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370839



Internal ID22193574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32910441..32916229hg38UCSC Ensembl
chr14:33379647..33385435hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385789
hg195789
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3234404
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370839
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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