A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456605



Internal ID22250822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109729225..109729307hg38UCSC Ensembl
chr13:110381572..110381654hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203325
Supporting Variants
SamplesHG00733
Known GenesLINC00676
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456605
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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