A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429263



Internal ID22170892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100420451..100420451hg38UCSC Ensembl
chr8:101432679..101432679hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg381919
hg191919
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3555758
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429263
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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