A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14438170



Internal ID22181285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61033314..61033463hg38UCSC Ensembl
chr8:61945873..61946022hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183310
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14438170
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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