A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380951



Internal ID22267065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83827838..83865454hg38UCSC Ensembl
chr15:84496590..84534206hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3837617
hg1937617
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3241058
Supporting Variants
SamplesNA19238
Known GenesADAMTSL3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380951
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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