A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390992



Internal ID22306193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2231789..2231845hg38UCSC Ensembl
chr10:2273983..2274039hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210273
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)nssv14390992
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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