A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202995



Internal ID22352080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75763434..75763746hg38UCSC Ensembl
chr11:75474479..75474791hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14415466, nssv14442665, nssv14386476
SamplesNA19240, HG00733, HG00514
Known GenesLOC283214
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202995
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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