A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008849



Internal ID21918192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10331210..10333244hg38UCSC Ensembl
chr8:10188720..10190754hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382035
hg192035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577332
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008849
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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