A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14410032



Internal ID22291038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:867474..867545hg38UCSC Ensembl
chr4:861262..861333hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3173054
Supporting Variants
SamplesNA19240
Known GenesGAK
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14410032
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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