A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14417439



Internal ID22153650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112164021..112164096hg38UCSC Ensembl
chr13:112818335..112818410hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195366
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)nssv14417439
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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