A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402678



Internal ID22330688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73575271..73575372hg38UCSC Ensembl
chr13:74149408..74149509hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3285641
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)nssv14402678
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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