A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076917



Internal ID21986150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177751134..177751134hg38UCSC Ensembl
chr3:177468922..177468922hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557112
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076917
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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