A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14318569



Internal ID22317861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165508843..165508970hg38UCSC Ensembl
chr4:166429995..166430122hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203788
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14318569
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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