A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582292



Internal ID21774335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73919224..73919286hg38UCSC Ensembl
chr10:75678982..75679044hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019861
Supporting Variants
Samples
Known GenesC10orf55
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582292
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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