A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14464606



Internal ID22215747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35842226..35842339hg38UCSC Ensembl
chr6:35810003..35810116hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183744
Supporting Variants
SamplesHG00733
Known GenesSRPK1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14464606
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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