A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414943



Internal ID22150415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14602478..14602618hg38UCSC Ensembl
chr10:14644477..14644617hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209483
Supporting Variants
SamplesHG00514
Known GenesFAM107B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414943
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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