A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216681



Internal ID22362595
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285914
SamplesHG00731
Known GenesADAMTS10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216681
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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