A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586088



Internal ID21778131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112913205..112913261hg38UCSC Ensembl
chr10:114672964..114673020hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586088
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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