A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299547



Internal ID22273098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52167425..52167493hg38UCSC Ensembl
chr20:50783964..50784032hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3534336
Supporting Variants
SamplesNA19239
Known GenesZFP64
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299547
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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