A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379737



Internal ID22172789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96866677..96871890hg38UCSC Ensembl
chr15:97409907..97415120hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385214
hg195214
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246889
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379737
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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