A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608639



Internal ID21556944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37157989..37157989hg38UCSC Ensembl
chr3:37199480..37199480hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124712
SamplesHG03009
Known GenesLRRFIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608639
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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