A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582797



Internal ID21774840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128136228..128136363hg38UCSC Ensembl
chr10:129934492..129934627hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582797
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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