A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14440308



Internal ID22236863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95691334..95691553hg38UCSC Ensembl
chr10:97451091..97451310hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206371
Supporting Variants
SamplesHG00733
Known GenesTCTN3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14440308
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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