A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528415



Internal ID22397803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9284981..9286137hg38UCSC Ensembl
chr18:9284979..9286135hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14289922, nssv14289921
SamplesHG00731, HG00732
Known GenesANKRD12
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528415
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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