A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065348



Internal ID21974581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94362621..94362621hg38UCSC Ensembl
chr5:93698326..93698326hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547954
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065348
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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