A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456668



Internal ID22250879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3656336..3656392hg38UCSC Ensembl
chr16:3706337..3706393hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210164
Supporting Variants
SamplesHG00733
Known GenesDNASE1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456668
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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