A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439436



Internal ID22236157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134865501..134865572hg38UCSC Ensembl
chr8:135877744..135877815hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209341
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)nssv14439436
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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