A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14315443



Internal ID22272828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99862726..99862801hg38UCSC Ensembl
chr4:100783883..100783958hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205028
Supporting Variants
SamplesNA19239
Known GenesDAPP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14315443
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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