A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14333138



Internal ID22259037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741597hg38UCSC Ensembl
chr10:19030376..19030526hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220537
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14333138
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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