A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414731



Internal ID22150184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1584723..1584782hg38UCSC Ensembl
chr11:1605953..1606012hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209260
Supporting Variants
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)nssv14414731
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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