A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106754



Internal ID21426539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8590672..8590807hg38UCSC Ensembl
chr19:8655556..8655691hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599694
Supporting Variants
SamplesHG00731
Known GenesADAMTS10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106754
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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