A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14383586



Internal ID22293769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8186678..8186787hg38UCSC Ensembl
chr10:8228641..8228750hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202600
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14383586
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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