A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14440536



Internal ID22237049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123253719..123256320hg38UCSC Ensembl
chr10:125013235..125015836hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203244
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)nssv14440536
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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