A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069930



Internal ID21480584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18812860..18812909hg38UCSC Ensembl
chr10:19101789..19101838hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586037
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069930
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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