A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14440662



Internal ID22237154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165776035..165776133hg38UCSC Ensembl
chr1:165745272..165745370hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3176693
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)nssv14440662
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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