A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072942



Internal ID21982175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109000850..109000850hg38UCSC Ensembl
chr4:109922006..109922006hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549800
Samples
Known GenesCOL25A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072942
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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