A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015666



Internal ID21925009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127848014..127848071hg38UCSC Ensembl
chr10:129646278..129646335hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015666
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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