A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209260



Internal ID22357366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1584723..1584782hg38UCSC Ensembl
chr11:1605953..1606012hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1225n152
Supporting Variantsnssv14414731
SamplesHG00514
Known GenesKRTAP5-1, KRTAP5-AS1, MOB2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209260
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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