A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000973



Internal ID21910316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42903862..42903939hg38UCSC Ensembl
chr8:42759005..42759082hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589308
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000973
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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