A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069864



Internal ID21440489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43697193..43697193hg38UCSC Ensembl
chr10:44192641..44192641hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637055
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069864
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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