A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465305



Internal ID22217613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82259963..82270217hg38UCSC Ensembl
chr6:82969680..82979934hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810255
hg1910255
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182295
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)nssv14465305
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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