A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354599



Internal ID22195439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114138084..114138310hg38UCSC Ensembl
chr10:115897843..115898069hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228492
Supporting Variants
SamplesHG00731
Known GenesC10orf118
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354599
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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