A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352939



Internal ID22329448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100343067..100343815hg38UCSC Ensembl
chr10:102102824..102103572hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227216
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352939
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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