A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216219



Internal ID22362285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76757318..76757830hg38UCSC Ensembl
chr14:77223661..77224173hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372232
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216219
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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