A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225933



Internal ID22368915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96320564..96321251hg38UCSC Ensembl
chr15:96863793..96864480hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378828
SamplesHG00731
Known GenesNR2F2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225933
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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