A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071091



Internal ID21402178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60569088..60569088hg38UCSC Ensembl
chr10:62328846..62328846hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382565
hg192565
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639239
Supporting Variants
SamplesHG00096
Known GenesANK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071091
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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