A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14461002



Internal ID22213571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182830858..182835584hg38UCSC Ensembl
chr4:183752011..183756737hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3184462
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)nssv14461002
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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