A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011982



Internal ID21921325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121717966..121729674hg38UCSC Ensembl
chr10:123477480..123489189hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3811709
hg1911710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011982
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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