A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071920



Internal ID21476504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83989858..83989858hg38UCSC Ensembl
chr10:85749614..85749614hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635302
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071920
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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