A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338855



Internal ID22123840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156941435..156941945hg38UCSC Ensembl
chr7:156734129..156734639hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216440
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338855
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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