A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947939



Internal ID22723431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9932375..9932375hg38UCSC Ensembl
chr3:9974059..9974059hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420557
Samples
Known GenesIL17RC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947939
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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