A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760797



Internal ID20536657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142785799..142785799hg38UCSC Ensembl
chr6:143106936..143106936hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273931
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760797
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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