A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14440732



Internal ID22237219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181426709..181426709hg38UCSC Ensembl
chr1:181395845..181395845hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3535467
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)nssv14440732
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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