A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590260



Internal ID21782303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29619486..29623428hg38UCSC Ensembl
chr10:29908415..29912357hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383943
hg193943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020370
Supporting Variants
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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