A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173329



Internal ID22332270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93602516..93602878hg38UCSC Ensembl
chr5:92938222..92938584hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14426679
SamplesHG00514
Known GenesMIR548AO
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173329
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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