A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316930



Internal ID22190856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108407932..108408748hg38UCSC Ensembl
chr4:109329088..109329904hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201570
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316930
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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