A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14438676



Internal ID22232742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135713409..135815598hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38102190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196165
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)nssv14438676
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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