A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071149



Internal ID21456387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69332357..69332357hg38UCSC Ensembl
chr10:71092113..71092113hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624686
Supporting Variants
SamplesHG02492
Known GenesHK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071149
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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