A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228186



Internal ID22370454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42350281..42350807hg38UCSC Ensembl
chr15:42642479..42643005hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377075, nssv14383719
SamplesNA19238, NA19240
Known GenesGANC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228186
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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