A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442863



Internal ID22239058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36287104..36287159hg38UCSC Ensembl
chr11:36308654..36308709hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208679
Supporting Variants
SamplesHG00733
Known GenesCOMMD9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14442863
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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