A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007169



Internal ID21916512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43965050..43969982hg38UCSC Ensembl
chr8:43820193..43825125hg19UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007169
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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