A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452931



Internal ID22218318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:775144..781885hg38UCSC Ensembl
chr10:821084..827825hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg386742
hg196742
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206986
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)nssv14452931
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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