A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076364



Internal ID21985597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90906879..90906879hg38UCSC Ensembl
chr8:91919107..91919107hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590028
Samples
Known GenesNECAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076364
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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