A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338885



Internal ID22123902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157411163..157411163hg38UCSC Ensembl
chr7:157203857..157203857hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565072
Supporting Variants
SamplesHG00512
Known GenesDNAJB6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338885
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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