A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078560



Internal ID21987793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26484866..26484866hg38UCSC Ensembl
chr4:26486488..26486488hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538024
Samples
Known GenesCCKAR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078560
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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