A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384074



Internal ID22319371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150322298..150326704hg38UCSC Ensembl
chr6:150643434..150647840hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384407
hg194407
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3185433
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)nssv14384074
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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