A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351387



Internal ID22158568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63664771..63672743hg38UCSC Ensembl
chr10:65424531..65432503hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387973
hg197973
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527684
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351387
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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