A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594580



Internal ID21786623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16595877..16595948hg38UCSC Ensembl
chr10:16637876..16637947hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011218
Supporting Variants
Samples
Known GenesRSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594580
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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