A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14458771



Internal ID22252582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79812323..79812625hg38UCSC Ensembl
chr17:77786122..77786424hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200570
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)nssv14458771
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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