A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003155



Internal ID21912498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92474232..92474444hg38UCSC Ensembl
chr10:94233989..94234201hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594559
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003155
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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