A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311784



Internal ID22265686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2334744..2334826hg38UCSC Ensembl
chr4:2336471..2336553hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203114
Supporting Variants
SamplesNA19238
Known GenesZFYVE28
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311784
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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