A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328363



Internal ID22193431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4441758..4441818hg38UCSC Ensembl
chr10:4483950..4484010hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529951
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328363
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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