A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581752



Internal ID21773795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23420967..23422732hg38UCSC Ensembl
chr10:23709896..23711661hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016166
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581752
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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