A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414149



Internal ID22149527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49302950..49303564hg38UCSC Ensembl
chr10:50510995..50511609hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199959
Supporting Variants
SamplesHG00514
Known GenesC10orf71
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414149
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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