A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381358



Internal ID22314839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21661527..21661749hg38UCSC Ensembl
chr10:21950456..21950678hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202288
Supporting Variants
SamplesNA19240
Known GenesMLLT10
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381358
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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