A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215138



Internal ID22361570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88009812..88009874hg38UCSC Ensembl
chr16:88043418..88043480hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378706
SamplesNA19238
Known GenesBANP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215138
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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