A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591968



Internal ID21784011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70220590..70220671hg38UCSC Ensembl
chr10:71980346..71980427hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012877
Supporting Variants
Samples
Known GenesPPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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