A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14444128



Internal ID22240153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27533754..27533754hg38UCSC Ensembl
chr13:28107891..28107891hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3546639
Supporting Variants
SamplesHG00733
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)nssv14444128
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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