A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132432



Internal ID21401265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112822777..112822777hg38UCSC Ensembl
chr3:112541624..112541624hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622619
Supporting Variants
SamplesHG00096
Known GenesCD200R1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132432
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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