A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461585



Internal ID22214171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87124552..87124735hg38UCSC Ensembl
chr16:87158158..87158341hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221887
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)nssv14461585
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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