A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354803



Internal ID22127462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83875281..83882622hg38UCSC Ensembl
chr10:85635037..85642378hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg387342
hg197342
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216311
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354803
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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