A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069131



Internal ID21978364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174629126..174629126hg38UCSC Ensembl
chr4:175550277..175550277hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069131
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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