A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076986



Internal ID21986219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186299773..186299773hg38UCSC Ensembl
chr4:187220927..187220927hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556686
Samples
Known GenesF11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076986
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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