A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14343832



Internal ID22143234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49335417..49335653hg38UCSC Ensembl
chr10:50543462..50543698hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528764
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14343832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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