A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359801



Internal ID22211343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63817238..63822357hg38UCSC Ensembl
chr11:63584710..63589829hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385120
hg195120
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236273
Supporting Variants
SamplesHG00732
Known GenesC11orf84
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359801
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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