A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452385



Internal ID22247299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134443404..134443685hg38UCSC Ensembl
chr4:135364559..135364840hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172383
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)nssv14452385
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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