A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077778



Internal ID21987011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177700890..177700890hg38UCSC Ensembl
chr3:177418678..177418678hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543391
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077778
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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