A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457583



Internal ID22251621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234644455..234650614hg38UCSC Ensembl
chr2:235553099..235559258hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg386160
hg196160
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3176955
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)nssv14457583
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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