A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078093



Internal ID21987326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76578872..76578872hg38UCSC Ensembl
chr5:75874697..75874697hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547671
Samples
Known GenesIQGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078093
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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