A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078920



Internal ID21988153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73644217..73644217hg38UCSC Ensembl
chr5:72940042..72940042hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539299
Samples
Known GenesARHGEF28
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078920
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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