A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14462860



Internal ID22215399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2585808..2585897hg38UCSC Ensembl
chr6:2586042..2586131hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3171429
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14462860
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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