A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075905



Internal ID21985138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109783815..109783815hg38UCSC Ensembl
chr4:110704971..110704971hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549427
Samples
Known GenesCFI
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075905
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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