A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14464859



Internal ID22217229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61610588..61610638hg38UCSC Ensembl
chr5:60906415..60906465hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179091
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)nssv14464859
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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