A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227149



Internal ID22369734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34790342..34790550hg38UCSC Ensembl
chr18:32370306..32370514hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283359
SamplesNA19239
Known GenesDTNA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227149
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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