A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14406361



Internal ID22322602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38855537..38855761hg38UCSC Ensembl
chr19:39346177..39346401hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3292092
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14406361
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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