A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000704



Internal ID21910047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69855799..69855874hg38UCSC Ensembl
chr8:70768034..70768109hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000704
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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