A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442570



Internal ID22228818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1584716..1584776hg38UCSC Ensembl
chr11:1605946..1606006hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197306
Supporting Variants
SamplesHG00733
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)nssv14442570
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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