A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14285914



Internal ID22190196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8590672..8590808hg38UCSC Ensembl
chr19:8655556..8655692hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216681
Supporting Variants
SamplesHG00731
Known GenesADAMTS10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14285914
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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