A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455588



Internal ID22249982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35092844..35093031hg38UCSC Ensembl
chr5:35092946..35093133hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3184320
Supporting Variants
SamplesHG00733
Known GenesPRLR
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455588
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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