A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14423491



Internal ID22162477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58786706..58787512hg38UCSC Ensembl
chr3:58772433..58773239hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180771
Supporting Variants
SamplesHG00514
Known GenesC3orf67
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14423491
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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