A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354350



Internal ID22127150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73777842..73778150hg38UCSC Ensembl
chr10:75537600..75537908hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220476
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354350
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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