A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356314



Internal ID22236906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92855255..92860290hg38UCSC Ensembl
chr10:94615012..94620047hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385036
hg195036
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223720
Supporting Variants
SamplesHG00733
Known GenesEXOC6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356314
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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