A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011809



Internal ID21921152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17226142..17226420hg38UCSC Ensembl
chr10:17268141..17268419hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583952
Samples
Known GenesVIM-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011809
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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