A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964237



Internal ID22739172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9926173..9926173hg38UCSC Ensembl
chr3:9967857..9967857hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423362
Samples
Known GenesIL17RC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964237
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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