A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456866



Internal ID22251041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8411206..8413654hg38UCSC Ensembl
chr3:8452892..8455340hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382449
hg192449
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174174
Supporting Variants
SamplesHG00733
Known GenesLMCD1-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456866
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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