A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032490



Internal ID21941833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88710605..88710668hg38UCSC Ensembl
chr16:88777013..88777076hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637319
Samples
Known GenesCTU2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032490
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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