A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14413077



Internal ID22148339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3693958..3694028hg38UCSC Ensembl
chr1:3610522..3610592hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186314
Supporting Variants
SamplesHG00514
Known GenesTP73
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14413077
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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