A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605183



Internal ID21553488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9932375..9932375hg38UCSC Ensembl
chr3:9974059..9974059hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128639
SamplesHG02818
Known GenesIL17RC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605183
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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