A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354470



Internal ID22290747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110747786..110747852hg38UCSC Ensembl
chr10:112507544..112507610hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227922
Supporting Variants
SamplesNA19240
Known GenesRBM20
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354470
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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