A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016714



Internal ID21926057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101728922..101734459hg38UCSC Ensembl
chr10:103488679..103494216hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385538
hg195538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016714
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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