A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375896



Internal ID22125718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95502622..95506314hg38UCSC Ensembl
chr14:95968959..95972651hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383693
hg193693
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3233381
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375896
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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