A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14413555



Internal ID22148865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986781..32988365hg38UCSC Ensembl
chr1:33452382..33453966hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381585
hg191585
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170632
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14413555
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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