A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765866



Internal ID20541726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6659300..6659300hg38UCSC Ensembl
chr5:6659413..6659413hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279629
Samples
Known GenesSRD5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765866
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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