A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226725



Internal ID22369435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18378060..18524928hg38UCSC Ensembl
chr11:18399607..18546475hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38146869
hg19146869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355468
SamplesHG00732
Known GenesLDHA, LDHAL6A, LDHC, TSG101
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226725
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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