A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002812



Internal ID21912155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33598392..33598463hg38UCSC Ensembl
chr8:33455910..33455981hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576618
Samples
Known GenesDUSP26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002812
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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