A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314908



Internal ID22205216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38880090..38880145hg38UCSC Ensembl
chr4:38881711..38881766hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192853
Supporting Variants
SamplesHG00732
Known GenesFAM114A1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314908
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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