A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14426869



Internal ID22167442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50939844..50939894hg38UCSC Ensembl
chr6:50907557..50907607hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3173989
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14426869
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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