A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14449065



Internal ID22244425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42915547..42915673hg38UCSC Ensembl
chr1:43381218..43381344hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180426
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14449065
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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