A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200576



Internal ID22350002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126473080..126473130hg38UCSC Ensembl
chr11:126342975..126343025hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1619n152
Supporting Variantsnssv14415601, nssv14381157
SamplesNA19240, HG00514
Known GenesKIRREL3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200576
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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