A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068630



Internal ID21977863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57126127..57126127hg38UCSC Ensembl
chr3:57160155..57160155hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538898
Samples
Known GenesIL17RD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068630
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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