A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529645



Internal ID22399036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49254388..49255181hg38UCSC Ensembl
chr16:49288299..49289092hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387943
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529645
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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