A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14343128



Internal ID22242448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39466301..39469450hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383150
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224059
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14343128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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