A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186554



Internal ID22339262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76336057..76336108hg38UCSC Ensembl
chr5:75631882..75631933hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7385n152
Supporting Variantsnssv14436116
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186554
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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