A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066653



Internal ID21975886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97775708..97775708hg38UCSC Ensembl
chr8:98787936..98787936hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582596
Samples
Known GenesLAPTM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066653
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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