A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453406



Internal ID22248164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157309853..157314391hg38UCSC Ensembl
chr6:157730885..157735423hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384539
hg194539
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3171779
Supporting Variants
SamplesHG00733
Known GenesTMEM242
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453406
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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