A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071183



Internal ID21980416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55360233..55360233hg38UCSC Ensembl
chr4:56226400..56226400hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545325
Samples
Known GenesSRD5A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071183
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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