A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407256



Internal ID22313501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11959476..11959552hg38UCSC Ensembl
chr18:11959475..11959551hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3292471
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)nssv14407256
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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