A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384832



Internal ID22298192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7856583..7856645hg38UCSC Ensembl
chr1:7916643..7916705hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3175537
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14384832
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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