A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14311302



Internal ID22277688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7752960..7752960hg38UCSC Ensembl
chr4:7754687..7754687hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563485
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14311302
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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