A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466657



Internal ID22218899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96367467..96367598hg38UCSC Ensembl
chr8:97379695..97379826hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209571
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14466657
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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