A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198910



Internal ID22348576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131679409..131682818hg38UCSC Ensembl
chr11:131549303..131552712hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1637n152
Supporting Variantsnssv14376754, nssv14382129
SamplesNA19240
Known GenesNTM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198910
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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