A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588194



Internal ID21780237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93812485..93813131hg38UCSC Ensembl
chr10:95572242..95572888hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588194
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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