A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218629



Internal ID22363916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67041185..67041243hg38UCSC Ensembl
chr15:67333523..67333581hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14388509
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218629
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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