A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356048



Internal ID22283693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128209288..128209339hg38UCSC Ensembl
chr10:130007552..130007603hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528492
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356048
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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